Allele Registry

Canonical Allele Identifier: PA2826401426

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000020031

RCV001218475

ClinVar Variation:

18363

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243586.1:p.Ser274Phe	CA128062 NM_001256657.2:c.821C>T