Allele Registry

Canonical Allele Identifier: PA126127

Gene: GC HGNC NCBI

ClinVar RCV:

RCV000017356

RCV003315503

ClinVar Variation:

15986

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191235.1:p.Thr436Lys	CA126125 NM_001204306.1:c.1307C>A