Canonical Allele Identifier: PA100746
Gene: GP1BA HGNC NCBI

Linked Data

ClinVar Variation Id: 4156

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000164.5:p.Ala172Val
CA116662
NM_000173.7:c.515C>T