Canonical Allele Identifier: PA1139680209
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 835938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000742.1:p.Asp440Val
CA2168322
NM_000751.2:c.1319A>T