Canonical Allele Identifier: PA2825754086
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 545009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124451.1:p.Leu587Pro
CA1705913
NM_001130979.2:c.1760T>C