Allele Registry

Canonical Allele Identifier: PA2826401405

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000538556

RCV001357055

ClinVar Variation:

466196

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243586.1:p.Arg228His	CA2168126 NM_001256657.2:c.683G>A