Canonical Allele Identifier: PA645377300
Gene: GP1BA HGNC NCBI

Linked Data

ClinVar Variation Id: 226006

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000164.5:p.Thr161Met
CA8314782
NM_000173.7:c.482C>T