Allele Registry

Canonical Allele Identifier: PA2826942307

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV001036943

RCV004031012

ClinVar Variation:

835938

HGVS (amino-acid)	Matching Registered Transcripts
NP_001298124.1:p.Asp246Val	CA2168322 NM_001311195.2:c.737A>T