Canonical Allele Identifier: PA2825750040
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 955036
ClinVar RCV Id: RCV001227601 RCV001833966
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.His1012Pro
CA347216979
NM_001130977.2:c.3035A>C