Canonical Allele Identifier: PA2580111254
Gene: GP1BB HGNC NCBI

Linked Data

ClinVar Variation Id: 2323735
ClinVar RCV Id: RCV004165097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000398.1:p.Leu166Met
CA410677626
NM_000407.5:c.496T>A