Canonical Allele Identifier: PA658811681
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 500669
ClinVar RCV Id: RCV000592042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Ser31Cys
CA350682818
NM_001927.4:c.91A>T