Allele Registry

Canonical Allele Identifier: PA095752

Gene: GCDH HGNC NCBI

ClinVar Allele:

17127

ClinVar RCV:

RCV000002169

RCV000224327

RCV002512671

ClinVar Variation:

2088

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Val400Met	CA252099 NM_000159.4:c.1198G>A