Canonical Allele Identifier: PA2828914850
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1393027
ClinVar RCV Id: RCV001896521 RCV003146313
ClinVar Variation Id: 2943907
ClinVar RCV Id: RCV003803465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369637.1:p.Phe35Leu
CA2125020
NM_001382708.1:c.105C>A
CA350682905
NM_001382708.1:c.103T>C
CA350682917
NM_001382708.1:c.105C>G