Canonical Allele Identifier: PA658806739
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 545009
ClinVar RCV Id: RCV000656079 RCV001089586 RCV001220606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Leu574Pro
CA1705913
NM_001130987.2:c.1721T>C