Canonical Allele Identifier: PA2828915326
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1393027
ClinVar Variation Id: 2943907
ClinVar RCV Id: RCV003803465

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369638.1:p.Phe35Leu
CA2125020
NM_001382709.1:c.105C>A
CA350682905
NM_001382709.1:c.103T>C
CA350682917
NM_001382709.1:c.105C>G