Allele Registry

Canonical Allele Identifier: PA126128

Gene: GC HGNC NCBI

ClinVar RCV:

RCV000017356

RCV003315503

ClinVar Variation:

15986

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191236.1:p.Thr455Lys	CA126125 NM_001204307.1:c.1364C>A