Canonical Allele Identifier: PA2826942308
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 1944674
ClinVar RCV Id: RCV002639897

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001298124.1:p.Ala248Val
CA351005708
NM_001311195.2:c.743C>T