Canonical Allele Identifier: PA2825749031
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 284469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Val69Gly
CA10604804
NM_001130977.2:c.206T>G