Allele Registry

Canonical Allele Identifier: PA110494

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000020031

RCV001218475

ClinVar Variation:

18363

HGVS (amino-acid)	Matching Registered Transcripts
NP_000742.1:p.Ser289Phe	CA128062 NM_000751.2:c.866C>T