Canonical Allele Identifier: PA2825764602
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2162951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124456.1:p.Met395Leu
CA16609661
NM_001130984.2:c.1183A>C
CA347213685
NM_001130984.2:c.1183A>T