Allele Registry

Canonical Allele Identifier: PA2825070223

Gene: GCDH HGNC NCBI

ClinVar Allele:

3062687

ClinVar RCV:

RCV003603772

ClinVar Variation:

2907540

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Gly354Cys	CA404320276 NM_000159.4:c.1060G>T