Canonical Allele Identifier: PA2828917276
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1677711
ClinVar RCV Id: RCV002224453 RCV004047210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369642.1:p.Asn198Lys
CA350691670
NM_001382713.1:c.594C>A
CA350691672
NM_001382713.1:c.594C>G