Allele Registry

Canonical Allele Identifier: PA2829730387

Gene: PIGN HGNC NCBI

ClinVar RCV:

RCV001212943

ClinVar Variation:

942868

HGVS (amino-acid)	Matching Registered Transcripts
NP_036459.1:p.His188Asn	CA402602309 NM_012327.6:c.562C>A