Allele Registry

Canonical Allele Identifier: PA126132

Gene: GC HGNC NCBI

ClinVar Allele:

31026

ClinVar RCV:

RCV000017357

RCV003992157

ClinVar Variation:

15987

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191236.1:p.Asp451Glu	CA126129 NM_001204307.1:c.1353T>G CA357201274 NM_001204307.1:c.1353T>A