Canonical Allele Identifier: PA645498557
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 411152
ClinVar RCV Id: RCV000473464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Leu470Phe
CA16610675
NM_001927.4:c.1408C>T