Canonical Allele Identifier: PA222179
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 94332
ClinVar RCV Id: RCV000080298 RCV000669830 RCV000864868 RCV001086563 RCV003952509
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Val1626Ile
CA222178
NM_003494.4:c.4876G>A