Allele Registry

Canonical Allele Identifier: PA2573255982

Gene: GCDH HGNC NCBI

ClinVar RCV:

RCV001996365

ClinVar Variation:

1498017

HGVS (amino-acid)	Matching Registered Transcripts
NP_039663.1:p.Arg227Leu	CA404318600 NM_013976.3:c.680G>T