Allele Registry

Canonical Allele Identifier: PA916009214

Gene: GCDH HGNC NCBI

ClinVar Variation Id: 656532

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Met366Ile	CA404321257 NM_013976.3:c.1098G>A CA404321258 NM_013976.3:c.1098G>C CA404321259 NM_013976.3:c.1098G>T