Canonical Allele Identifier: PA658811834
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 497856
ClinVar RCV Id: RCV000595412 RCV000796751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Ile367Thr
CA350694218
NM_001927.4:c.1100T>C