Canonical Allele Identifier: PA133828
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 44251
ClinVar RCV Id: RCV000037231 RCV001852772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Gly456Arg
CA133826
NM_001927.4:c.1366G>A
CA350698798
NM_001927.4:c.1366G>C