Canonical Allele Identifier: PA2825748386
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_001124448.1:p.Ala1545Thr
CA1707145
NM_001130976.2:c.4633G>A