Canonical Allele Identifier: PA2825765982
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 471315
ClinVar RCV Id: RCV000532679 RCV001834797 RCV004024174
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124456.1:p.Arg1685His
CA1707257
NM_001130984.2:c.5054G>A