NM_002591.4(PCK1):c.556G>A (p.Asp186Asn) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 7, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004021840.1
Allele description [Variation Report for NM_002591.4(PCK1):c.556G>A (p.Asp186Asn)]
NM_002591.4(PCK1):c.556G>A (p.Asp186Asn)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Mus musculus actin, beta-like 2, mRNA (cDNA clone MGC:132977 IMAGE:40062276), co...
Mus musculus actin, beta-like 2, mRNA (cDNA clone MGC:132977 IMAGE:40062276), complete cdsgi|109730634|gb|BC112429.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024