Allele Registry

Canonical Allele Identifier: PA2826401307

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000020037

ClinVar Variation:

18369

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243586.1:p.Phe80Leu	CA128069 NM_001256657.2:c.238T>C CA350997468 NM_001256657.2:c.240T>A CA350997469 NM_001256657.2:c.240T>G