Allele Registry

Canonical Allele Identifier: PA126126

Gene: GC HGNC NCBI

ClinVar RCV:

RCV000017356

RCV003315503

ClinVar Variation:

15986

HGVS (amino-acid)	Matching Registered Transcripts
NP_000574.2:p.Thr436Lys	CA126125 NM_000583.4:c.1307C>A