Canonical Allele Identifier: PA1139719604
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 840172
ClinVar RCV Id: RCV001042104
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Met381Thr
CA2125247
NM_001927.4:c.1142T>C