Allele Registry

Canonical Allele Identifier: PA916021163

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000020031

RCV001218475

ClinVar Variation:

18363

HGVS (amino-acid)	Matching Registered Transcripts
NP_001298124.1:p.Ser95Phe	CA128062 NM_001311195.2:c.284C>T