Canonical Allele Identifier: PA2825757238
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 1984899
ClinVar RCV Id: RCV002775735
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124452.1:p.Val1376Ile
CA1706899
NM_001130980.2:c.4126G>A