Canonical Allele Identifier: PA645497805
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 421688
ClinVar RCV Id: RCV000484348 RCV001240419 RCV002323831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Val110Leu
CA2125052
NM_001927.4:c.328G>C
CA350685264
NM_001927.4:c.328G>T