Canonical Allele Identifier: PA2580111244
Gene: GP1BB HGNC NCBI

Linked Data

ClinVar Variation Id: 2432237

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000398.1:p.Leu146Phe
CA410677507
NM_000407.5:c.436C>T