Canonical Allele Identifier: PA2499232218
Gene: GP1BB HGNC NCBI

Linked Data

ClinVar Variation Id: 1034192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000398.1:p.Pro72Leu
CA10102331
NM_000407.5:c.215C>T