Canonical Allele Identifier: PA2825765635
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 500922
ClinVar RCV Id: RCV000591033 RCV002491213 RCV003574784
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124456.1:p.Cys1348Arg
CA1706900
NM_001130984.2:c.4042T>C