Canonical Allele Identifier: PA2825767469
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 196175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Tyr1032Cys
CA275155
NM_001130985.2:c.3095A>G