Allele Registry

Canonical Allele Identifier: PA2829730389

Gene: PIGN HGNC NCBI

ClinVar RCV:

RCV000481779

RCV001204694

ClinVar Variation:

422474

HGVS (amino-acid)	Matching Registered Transcripts
NP_036459.1:p.His188Tyr	CA8982544 NM_012327.6:c.562C>T