Canonical Allele Identifier: PA2825770254
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 285356
ClinVar RCV Id: RCV000530924 RCV000664797 RCV000725642 RCV003235177
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124458.1:p.Tyr1481His
CA1707060
NM_001130986.2:c.4441T>C