Canonical Allele Identifier: PA2825752916
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 471310
ClinVar RCV Id: RCV000732545 RCV000559661
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124450.1:p.Ala1580Thr
CA1707145
NM_001130978.2:c.4738G>A