Canonical Allele Identifier: PA2573062553
Gene: GP1BB HGNC NCBI

Linked Data

ClinVar Variation Id: 1338344
ClinVar RCV Id: RCV001817715

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000398.1:p.Pro99Leu
CA410677059
NM_000407.5:c.296C>T