Allele Registry

Canonical Allele Identifier: PA1139747217

Gene: PIGN HGNC NCBI

ClinVar RCV:

RCV001212943

ClinVar Variation:

942868

HGVS (amino-acid)	Matching Registered Transcripts
NP_789744.1:p.His188Asn	CA402602309 NM_176787.5:c.562C>A