Canonical Allele Identifier: PA2828915128
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_001369637.1:p.Asn287Lys
CA350691670
NM_001382708.1:c.861C>A
CA350691672
NM_001382708.1:c.861C>G