Canonical Allele Identifier: PA2825746769
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 579361
ClinVar RCV Id: RCV000702622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Val68Met
CA1705254
NM_001130976.2:c.202G>A