Allele Registry

Canonical Allele Identifier: PA095428

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000634889

ClinVar Variation:

529446

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Arg94Leu	CA404315814 NM_000159.4:c.281G>T