Allele Registry

Canonical Allele Identifier: PA2826942213

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000352373

RCV000808385

RCV003144223

ClinVar Variation:

334968

HGVS (amino-acid)	Matching Registered Transcripts
NP_001298124.1:p.Arg104His	CA2168184 NM_001311195.2:c.311G>A