Allele Registry

Canonical Allele Identifier: PA916009164

Gene: GCDH HGNC NCBI

ClinVar Allele:

189179

ClinVar RCV:

RCV000171557

ClinVar Variation:

191374

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Pro286Ser	CA274776 NM_013976.3:c.856C>T