Canonical Allele Identifier: PA2825768274
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 290354

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Thr1736Pro
CA1707307
NM_001130985.2:c.5206A>C