Allele Registry

Canonical Allele Identifier: PA916009229

Gene: GCDH HGNC NCBI

ClinVar Allele:

187043

ClinVar RCV:

RCV000169204

RCV004017449

ClinVar Variation:

188852

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Arg383Cys	CA274040 NM_013976.3:c.1147C>T