Canonical Allele Identifier: PA658811662
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 541304
ClinVar RCV Id: RCV000651549 RCV000730717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Ser13Tyr
CA350682283
NM_001927.4:c.38C>A