Allele Registry

Canonical Allele Identifier: PA916009255

Gene: GCDH HGNC NCBI

ClinVar Allele:

358602

ClinVar RCV:

RCV000411911

ClinVar Variation:

371251

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Gly390Ala	CA16041974 NM_013976.3:c.1169G>C