Allele Registry

Canonical Allele Identifier: PA2826942462

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000020031

RCV001218475

ClinVar Variation:

18363

HGVS (amino-acid)	Matching Registered Transcripts
NP_001298125.1:p.Ser188Phe	CA128062 NM_001311196.2:c.563C>T