Canonical Allele Identifier: PA2825747262
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 969695
ClinVar RCV Id: RCV001245099 RCV001835223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Pro524Thr
CA1705879
NM_001130976.2:c.1570C>A