Canonical Allele Identifier: PA2741812160
Gene: GP1BA HGNC NCBI

Linked Data

ClinVar Variation Id: 2682338
ClinVar RCV Id: RCV003479711

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000164.5:p.Thr469Ile
CA397321791
NM_000173.7:c.1406C>T