Canonical Allele Identifier: PA2825695890
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 452293
ClinVar RCV Id: RCV000520965 RCV001829524 RCV002528266
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Ala1974Val
CA1707565
NM_001130455.2:c.5921C>T