Canonical Allele Identifier: PA915965502
Gene: GP1BB HGNC NCBI

Linked Data

ClinVar Variation Id: 721649
ClinVar RCV Id: RCV000895183 RCV003479239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000398.1:p.Ala182Ser
CA322080121
NM_000407.5:c.544G>T