Allele Registry

Canonical Allele Identifier: PA658800966

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000642109

ClinVar Variation:

534526

HGVS (amino-acid)	Matching Registered Transcripts
NP_000742.1:p.Cys257Arg	CA66952998 NM_000751.2:c.769T>C