Canonical Allele Identifier: PA2828915490
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2450706
ClinVar RCV Id: RCV003177142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369638.1:p.Glu161Asp
CA350686583
NM_001382709.1:c.483G>C
CA350686585
NM_001382709.1:c.483G>T