Allele Registry

Canonical Allele Identifier: PA095712

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000002165

ClinVar Variation:

2084

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Thr416Ile	CA252096 NM_000159.4:c.1247C>T