Canonical Allele Identifier: PA2825765686
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 501040
ClinVar RCV Id: RCV000658870 RCV001196059 RCV001140901
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124456.1:p.Val1390Ile
CA1706946
NM_001130984.2:c.4168G>A