Allele Registry

Canonical Allele Identifier: PA1139747033

Gene: PIGN HGNC NCBI

ClinVar RCV:

RCV001068903

ClinVar Variation:

862222

HGVS (amino-acid)	Matching Registered Transcripts
NP_789744.1:p.Glu61Lys	CA402604291 NM_176787.5:c.181G>A