NM_000407.5(GP1BB):c.399C>T (p.Ala133=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000247854.7
Allele description [Variation Report for NM_000407.5(GP1BB):c.399C>T (p.Ala133=)]
NM_000407.5(GP1BB):c.399C>T (p.Ala133=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
130065[uid] (1)
Taxonomy
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024