Canonical Allele Identifier: PA2825766184
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 471318
ClinVar RCV Id: RCV000534201
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124456.1:p.Asp1863Val
CA347223572
NM_001130984.2:c.5588A>T