Allele Registry

Canonical Allele Identifier: PA2829730487

Gene: PIGN HGNC NCBI

ClinVar Allele:

415608

ClinVar RCV:

RCV000489201

RCV000532832

RCV000624007

ClinVar Variation:

426983

HGVS (amino-acid)	Matching Registered Transcripts
NP_036459.1:p.Leu311Trp	CA8982449 NM_012327.6:c.932T>G