Allele Registry

Canonical Allele Identifier: PA916009208

Gene: GCDH HGNC NCBI

ClinVar Allele:

187042

ClinVar RCV:

RCV000169320

ClinVar Variation:

188946

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Gly354Ser	CA274169 NM_013976.3:c.1060G>A