Allele Registry

Canonical Allele Identifier: PA645443978

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000352373

RCV000808385

RCV003144223

ClinVar Variation:

334968

HGVS (amino-acid)	Matching Registered Transcripts
NP_000742.1:p.Arg298His	CA2168184 NM_000751.2:c.893G>A