Canonical Allele Identifier: PA2573062556
Gene: GP1BB HGNC NCBI

Linked Data

ClinVar Variation Id: 1320932
ClinVar RCV Id: RCV001776911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000398.1:p.Ala182Thr
CA322080125
NM_000407.5:c.544G>A