Canonical Allele Identifier: PA915973888
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 282449
ClinVar RCV Id: RCV000351237 RCV000665378 RCV001297834 RCV003469226
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124454.1:p.Arg1071Trp
CA1706450
NM_001130982.2:c.3211C>T