Allele Registry

Canonical Allele Identifier: PA658676684

Gene: GCDH HGNC NCBI

ClinVar Allele:

468501

ClinVar RCV:

RCV000539888

ClinVar Variation:

459948

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Glu397Lys	CA404321719 NM_000159.4:c.1189G>A