Canonical Allele Identifier: PA2826401489
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 534533
ClinVar RCV Id: RCV000642118 RCV000731206 RCV001138498
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243586.1:p.Arg361Gln
CA2168272
NM_001256657.2:c.1082G>A