Canonical Allele Identifier: PA2825759494
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 289963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124453.1:p.Asn1368Ser
CA1706892
NM_001130981.2:c.4103A>G