Allele Registry

Canonical Allele Identifier: PA2825069938

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000625783

ClinVar Variation:

522644

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Glu181Gln	CA9234426 NM_000159.4:c.541G>C