Canonical Allele Identifier: PA2825749505
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2819412
ClinVar RCV Id: RCV003735193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Gly505Trp
CA347217357
NM_001130977.2:c.1513G>T