Canonical Allele Identifier: PA2825748514
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 471314
ClinVar RCV Id: RCV000554512 RCV001508442 RCV001834796
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Arg1663Cys
CA1707255
NM_001130976.2:c.4987C>T