Canonical Allele Identifier: PA2825759124
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 1442763
ClinVar RCV Id: RCV001953153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124453.1:p.Tyr1051Cys
CA347217037
NM_001130981.2:c.3152A>G