Canonical Allele Identifier: PA2825753245
Gene: DYSF HGNC NCBI
ClinVar RCV:
RCV000534201
ClinVar Variation:
471318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124450.1:p.Asp1876Val
CA347223572
NM_001130978.2:c.5627A>T