Canonical Allele Identifier: PA2825766468
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_001124457.1:p.Val69Met
CA1705254
NM_001130985.2:c.205G>A