Canonical Allele Identifier: PA2829466295
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 336950
ClinVar RCV Id: RCV000297254 RCV000392981 RCV000705827 RCV001828331
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Ala425Val
CA1705708
NM_003494.4:c.1274C>T