Canonical Allele Identifier: PA2825752862
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_001124450.1:p.Tyr1515His
CA1707060
NM_001130978.2:c.4543T>C