Canonical Allele Identifier: PA2825769075
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2162951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124458.1:p.Met395Leu
CA16609661
NM_001130986.2:c.1183A>C
CA347213685
NM_001130986.2:c.1183A>T