Allele Registry

Canonical Allele Identifier: PA2826942314

Gene: CHRND HGNC NCBI

ClinVar Allele:

450517

ClinVar RCV:

RCV000542114

RCV000762329

RCV001141061

ClinVar Variation:

466190

HGVS (amino-acid)	Matching Registered Transcripts
NP_001298124.1:p.Asn262Ser	CA2168330 NM_001311195.2:c.785A>G