Canonical Allele Identifier: PA2825754602
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 661790
ClinVar RCV Id: RCV000819285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124451.1:p.His1068Tyr
CA1706445
NM_001130979.2:c.3202C>T