Canonical Allele Identifier: PA2825749576
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2189797
ClinVar RCV Id: RCV002611827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Ser579Phe
CA1705967
NM_001130977.2:c.1736C>T