Allele Registry

Canonical Allele Identifier: PA2826401526

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV001036943

RCV004031012

ClinVar Variation:

835938

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243586.1:p.Asp425Val	CA2168322 NM_001256657.2:c.1274A>T