Canonical Allele Identifier: PA2825766947
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2819412
ClinVar RCV Id: RCV003735193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Gly537Trp
CA347217357
NM_001130985.2:c.1609G>T