Allele Registry

Canonical Allele Identifier: PA101090

Gene: GPI HGNC NCBI

ClinVar RCV:

RCV000014613

RCV001507434

ClinVar Variation:

13643

HGVS (amino-acid)	Matching Registered Transcripts
NP_000166.2:p.Thr224Met	CA123318 NM_000175.3:c.671C>T