Canonical Allele Identifier: PA2825695239
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 471311
ClinVar RCV Id: RCV000558437 RCV000592365 RCV001271549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Ile1608Val
CA1707194
NM_001130455.2:c.4822A>G