Canonical Allele Identifier: PA100783
Gene: GP1BA HGNC NCBI

Linked Data

ClinVar Variation Id: 4153
ClinVar RCV Id: RCV000004370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000164.5:p.Gly249Val
CA116659
NM_000173.7:c.746G>T