Allele Registry

Canonical Allele Identifier: PA916009568

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000020039

ClinVar Variation:

18371

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243586.1:p.Leu63Pro	CA128072 NM_001256657.2:c.188T>C