Canonical Allele Identifier: PA2825750078
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 6675
ClinVar RCV Id: RCV000007060 RCV000176936 RCV000763088 RCV000790688 RCV001229764
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Arg1032His
CA222152
NM_001130977.2:c.3095G>A