Allele Registry

Canonical Allele Identifier: PA2826942467

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000352373

RCV000808385

RCV003144223

ClinVar Variation:

334968

HGVS (amino-acid)	Matching Registered Transcripts
NP_001298125.1:p.Arg197His	CA2168184 NM_001311196.2:c.590G>A