Canonical Allele Identifier: PA275156
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 196175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Tyr1014Cys
CA275155
NM_003494.4:c.3041A>G