Allele Registry

Canonical Allele Identifier: PA2829730459

Gene: PIGN HGNC NCBI

ClinVar RCV:

RCV001351620

ClinVar Variation:

1046983

HGVS (amino-acid)	Matching Registered Transcripts
NP_036459.1:p.Ser270Thr	CA402601338 NM_012327.6:c.808T>A