Canonical Allele Identifier: PA2825748659
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 281104
ClinVar RCV Id: RCV000725163 RCV001085921 RCV003939934 RCV004021072 RCV001276862
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Arg1782Trp
CA1707403
NM_001130976.2:c.5344C>T