Allele Registry

Canonical Allele Identifier: PA2826942448

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000642109

ClinVar Variation:

534526

HGVS (amino-acid)	Matching Registered Transcripts
NP_001298125.1:p.Cys156Arg	CA66952998 NM_001311196.2:c.466T>C