Canonical Allele Identifier: PA2825768220
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 288830
ClinVar RCV Id: RCV000370944 RCV002518057
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Cys1696Tyr
CA10606239
NM_001130985.2:c.5087G>A