Canonical Allele Identifier: PA2825756848
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 955036

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124452.1:p.His1043Pro
CA347216979
NM_001130980.2:c.3128A>C