Canonical Allele Identifier: PA2829469100
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 501582
ClinVar RCV Id: RCV000596899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Cys1971Arg
CA347226529
NM_003494.4:c.5911T>C