Canonical Allele Identifier: PA2825761564
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 290354
ClinVar RCV Id: RCV000328882 RCV000557258 RCV001833407
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124454.1:p.Thr1750Pro
CA1707307
NM_001130982.2:c.5248A>C