Canonical Allele Identifier: PA658820705
Gene: GP1BA HGNC NCBI

Linked Data

ClinVar Variation Id: 2736404
ClinVar RCV Id: RCV003559937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000164.5:p.Leu195del
CA658820706
NM_000173.7:c.584_586del