Canonical Allele Identifier: PA2825750054
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 582986
ClinVar RCV Id: RCV000707195 RCV001830567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Thr1022Arg
CA49746708
NM_001130977.2:c.3065C>G