Canonical Allele Identifier: PA2825750505
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 288624
ClinVar RCV Id: RCV000358891 RCV001140902 RCV001833383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Arg1409Cys
CA1706966
NM_001130977.2:c.4225C>T