Canonical Allele Identifier: PA2825770726
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2201500
ClinVar RCV Id: RCV002654996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124458.1:p.Lys1924Glu
CA347226297
NM_001130986.2:c.5770A>G