Canonical Allele Identifier: PA891861097
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 582986

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Thr1054Arg
CA49746708
NM_001130987.2:c.3161C>G