Canonical Allele Identifier: PA2825749605
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2023880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Asp611Asn
CA1705980
NM_001130977.2:c.1831G>A