Canonical Allele Identifier: PA2825751016
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 282408
ClinVar RCV Id: RCV000317613 RCV000754725 RCV002521880
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Tyr1884His
CA1707485
NM_001130977.2:c.5650T>C