Canonical Allele Identifier: PA2825767228
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 283977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Arg826Gln
CA1706183
NM_001130985.2:c.2477G>A