Canonical Allele Identifier: PA2825763333
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 955680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124455.1:p.Glu1295Gly
CA347226584
NM_001130983.2:c.3884A>G