Canonical Allele Identifier: PA1139719426
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 838709
ClinVar RCV Id: RCV001040305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001918.3:p.Arg163_Val168dup
CA916081390
NM_001927.4:c.488_505dup