Allele Registry

Canonical Allele Identifier: PA2829730443

Gene: PIGN HGNC NCBI

ClinVar RCV:

RCV001310393

ClinVar Variation:

1012442

HGVS (amino-acid)	Matching Registered Transcripts
NP_036459.1:p.Asp252Gly	CA402601620 NM_012327.6:c.755A>G