Canonical Allele Identifier: PA2825746941
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 259085
ClinVar RCV Id: RCV000249294 RCV000532146 RCV000733997 RCV001833275
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Val226Met
CA1705456
NM_001130976.2:c.676G>A