Canonical Allele Identifier: PA2825692749
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 284816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Val69Leu
CA1705253
NM_001130455.2:c.205G>C
CA347216455
NM_001130455.2:c.205G>T