Allele Registry

Canonical Allele Identifier: PA2825069764

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV001990342

ClinVar Variation:

1465690

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Arg88Gly	CA404315542 NM_000159.4:c.262C>G