Allele Registry

Canonical Allele Identifier: PA658666453

Gene: CHRND HGNC NCBI

ClinVar Allele:

450517

ClinVar RCV:

RCV000542114

RCV000762329

RCV001141061

ClinVar Variation:

466190

HGVS (amino-acid)	Matching Registered Transcripts
NP_000742.1:p.Asn456Ser	CA2168330 NM_000751.2:c.1367A>G