Allele Registry

Canonical Allele Identifier: PA129327

Gene: PIGN HGNC NCBI

ClinVar RCV:

RCV000023506

ClinVar Variation:

30549

HGVS (amino-acid)	Matching Registered Transcripts
NP_789744.1:p.Arg709Gln	CA129326 NM_176787.5:c.2126G>A