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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACVR2A
(P49L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ACVR2A
(K94R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ACVR2A
(T131R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACVR2A
(R162G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACVR2A
(I115V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACVR2A
(V261M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACVR2A
(G191R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACVR2A
(N332T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACVR2A
(R255Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACVR2A
(I386T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ACVR2A
(V387L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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