Canonical Allele Identifier: PA645497854
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 228549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Val126Leu
CA10576589
NM_001927.4:c.376G>T
CA350685689
NM_001927.4:c.376G>C