Allele Registry

Canonical Allele Identifier: PA128065

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000020033

RCV003517129

ClinVar Variation:

18365

HGVS (amino-acid)	Matching Registered Transcripts
NP_000742.1:p.Ile79Lys	CA128064 NM_000751.2:c.236T>A