Canonical Allele Identifier: PA2828917318
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2691160
ClinVar RCV Id: RCV003487209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369642.1:p.Met256Leu
CA350693712
NM_001382713.1:c.766A>C
CA350693718
NM_001382713.1:c.766A>T