Canonical Allele Identifier: PA2825747798
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 661790
ClinVar RCV Id: RCV000819285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.His1023Tyr
CA1706445
NM_001130976.2:c.3067C>T