Allele Registry

Canonical Allele Identifier: PA2580129565

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV002794855

ClinVar Variation:

1981765

HGVS (amino-acid)	Matching Registered Transcripts
NP_000742.1:p.Ile79Thr	CA2167951 NM_000751.2:c.236T>C