Allele Registry

Canonical Allele Identifier: PA916009213

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000002167

RCV000224528

ClinVar Variation:

2086

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Glu365Lys	CA252098 NM_013976.3:c.1093G>A