Canonical Allele Identifier: PA2741815209
Gene: GP1BB HGNC NCBI

Linked Data

ClinVar Variation Id: 2557864
ClinVar RCV Id: RCV004327387
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000398.1:p.Ala140Ser
CA410677465
NM_000407.5:c.418G>T