Canonical Allele Identifier: PA915965484
Gene: GP1BB HGNC NCBI

Linked Data

ClinVar Variation Id: 731652
ClinVar RCV Id: RCV000906639 RCV002479042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000398.1:p.Gly40Glu
CA10102315
NM_000407.5:c.119G>A