Canonical Allele Identifier: PA915965501
Gene: GP1BB HGNC NCBI

Linked Data

ClinVar Variation Id: 627087
ClinVar RCV Id: RCV000851814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000398.1:p.Leu172Pro
CA322080104
NM_000407.5:c.515T>C