Allele Registry

Canonical Allele Identifier: PA916009168

Gene: GCDH HGNC NCBI

ClinVar Allele:

532724

ClinVar RCV:

RCV000634890

ClinVar Variation:

529447

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Arg294Leu	CA404319365 NM_013976.3:c.881G>T