Canonical Allele Identifier: PA2825765597
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 336969
ClinVar RCV Id: RCV000291639 RCV000419423 RCV001272842 RCV000346595 RCV001753802 RCV001080538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124456.1:p.Ile1312Val
CA1706842
NM_001130984.2:c.3934A>G