Canonical Allele Identifier: PA2825762498
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 596925
ClinVar RCV Id: RCV000732902 RCV002535298
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124455.1:p.Gly535Ser
CA1705878
NM_001130983.2:c.1603G>A