Canonical Allele Identifier: PA2828916621
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 956977
ClinVar RCV Id: RCV001229880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369641.1:p.Gly44Val
CA350683193
NM_001382712.1:c.131G>T