Canonical Allele Identifier: PA2828915663
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1355754
ClinVar RCV Id: RCV001867087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369639.1:p.Arg16Ser
CA350682339
NM_001382710.1:c.46C>A