Allele Registry

Canonical Allele Identifier: PA126131

Gene: GC HGNC NCBI

ClinVar Allele:

31026

ClinVar RCV:

RCV000017357

RCV003992157

ClinVar Variation:

15987

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191235.1:p.Asp432Glu	CA126129 NM_001204306.1:c.1296T>G CA357201274 NM_001204306.1:c.1296T>A