Canonical Allele Identifier: PA2741891029
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2922180
ClinVar RCV Id: RCV003785394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Asp186Asn
CA350687095
NM_001927.4:c.556G>A