Canonical Allele Identifier: PA2825762346
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 538630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124455.1:p.Arg388Gln
CA1705662
NM_001130983.2:c.1163G>A