Canonical Allele Identifier: PA2580111258
Gene: GP1BB HGNC NCBI

Linked Data

ClinVar Variation Id: 2377515
ClinVar RCV Id: RCV004215848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000398.1:p.Leu178Arg
CA410677697
NM_000407.5:c.533T>G