Allele Registry

Canonical Allele Identifier: PA916009269

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV000173982

RCV000414299

RCV003955020

ClinVar Variation:

193798

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Met405Val	CA274948 NM_013976.3:c.1213A>G