Allele Registry

Canonical Allele Identifier: PA916009283

Gene: GCDH HGNC NCBI

ClinVar Variation Id: 167133

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Glu414Lys	CA234086 NM_013976.3:c.1240G>A