Canonical Allele Identifier: PA2825163470
Gene: GP1BB HGNC NCBI

Linked Data

ClinVar Variation Id: 3101043
ClinVar RCV Id: RCV004387901
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000398.1:p.Ala182Val
CA410677717
NM_000407.5:c.545C>T