Allele Registry

Canonical Allele Identifier: PA658676622

Gene: GCDH HGNC NCBI

ClinVar Allele:

469399

ClinVar RCV:

RCV000533495

ClinVar Variation:

459949

HGVS (amino-acid)	Matching Registered Transcripts
NP_000150.1:p.Glu90Lys	CA305500200 NM_000159.4:c.268G>A