Allele Registry

Canonical Allele Identifier: PA658801491

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000634888

RCV004544826

ClinVar Variation:

529445

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Gln160Arg	CA404317639 NM_000159.4:c.479A>G