Canonical Allele Identifier: PA2825756266
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 282209

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124452.1:p.Met482Val
CA1705737
NM_001130980.2:c.1444A>G