Canonical Allele Identifier: PA2825749306
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 287822
ClinVar RCV Id: RCV000329171 RCV001833378 RCV001247468
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Ala315Thr
CA1705596
NM_001130977.2:c.943G>A