Canonical Allele Identifier: PA2573169427
Gene: GP1BB HGNC NCBI

Linked Data

ClinVar Variation Id: 1684331
ClinVar RCV Id: RCV002245337

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000398.1:p.Gly149Arg
CA410677528
NM_000407.5:c.445G>A
CA410677529
NM_000407.5:c.445G>C