Allele Registry

Canonical Allele Identifier: PA095317

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000169226

RCV000480428

ClinVar Variation:

188872

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Arg257Trp	CA274064 NM_000159.4:c.769C>T