Allele Registry

Canonical Allele Identifier: PA2826401412

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000642109

ClinVar Variation:

534526

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243586.1:p.Cys242Arg	CA66952998 NM_001256657.2:c.724T>C