Canonical Allele Identifier: PA2825696067
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 896081
ClinVar RCV Id: RCV001138530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Leu2076Val
CA347227885
NM_001130455.2:c.6226C>G