Allele Registry

Canonical Allele Identifier: PA2826942562

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV001036943

RCV004031012

ClinVar Variation:

835938

HGVS (amino-acid)	Matching Registered Transcripts
NP_001298125.1:p.Asp339Val	CA2168322 NM_001311196.2:c.1016A>T