Canonical Allele Identifier: PA2825751099
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 381677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Pro1977Ser
CA16604254
NM_001130977.2:c.5929C>T