Canonical Allele Identifier: PA2826401527
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 1944674
ClinVar RCV Id: RCV002639897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243586.1:p.Ala427Val
CA351005708
NM_001256657.2:c.1280C>T