Canonical Allele Identifier: PA915965489
Gene: GP1BB HGNC NCBI

Linked Data

ClinVar Variation Id: 627272
ClinVar RCV Id: RCV000852068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000398.1:p.Pro71Leu
CA410676737
NM_000407.5:c.212C>T