Allele Registry

Canonical Allele Identifier: PA351606

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000207408

ClinVar Variation:

221907

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Thr344Ile	CA351605 NM_000159.4:c.1031C>T