Allele Registry

Canonical Allele Identifier: PA275978

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000190518

RCV000281284

RCV001682897

RCV001729448

ClinVar Variation:

208504

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Gln417Arg	CA275977 NM_013976.3:c.1250A>G