Canonical Allele Identifier: PA2825757470
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 501558
ClinVar RCV Id: RCV000594913 RCV000797230
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124452.1:p.Ala1589Thr
CA1707154
NM_001130980.2:c.4765G>A