Allele Registry

Canonical Allele Identifier: PA2826942480

Gene: CHRND HGNC NCBI

ClinVar RCV:

RCV000413500

RCV000532746

RCV003144251

RCV004022175

ClinVar Variation:

373561

HGVS (amino-acid)	Matching Registered Transcripts
NP_001298125.1:p.Gly215Ser	CA2168214 NM_001311196.2:c.643G>A