Allele Registry

Canonical Allele Identifier: PA916009233

Gene: GCDH HGNC NCBI

ClinVar Allele:

98436

ClinVar RCV:

RCV000078248

RCV000812634

ClinVar Variation:

92527

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Arg386Pro	CA220428 NM_013976.3:c.1157G>C