Canonical Allele Identifier: PA2825759106
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 284003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124453.1:p.Pro1037Leu
CA1706432
NM_001130981.2:c.3110C>T