Canonical Allele Identifier: PA2828915319
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1425184
ClinVar RCV Id: RCV001924330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369638.1:p.Pro25Leu
CA350682650
NM_001382709.1:c.74C>T
CA2573135504
NM_001382709.1:c.74_75delinsTG