Allele Registry

Canonical Allele Identifier: PA2825070026

Gene: GCDH HGNC NCBI

ClinVar Allele:

1372657

ClinVar RCV:

RCV001996365

ClinVar Variation:

1498017

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Arg227Leu	CA404318600 NM_000159.4:c.680G>T