Allele Registry

Canonical Allele Identifier: PA916009077

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000409563

ClinVar Variation:

371271

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Gly178Arg	CA9234423 NM_013976.3:c.532G>A CA404317989 NM_013976.3:c.532G>C