Canonical Allele Identifier: PA2825761799
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 647886

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124454.1:p.Ala1971Thr
CA1707553
NM_001130982.2:c.5911G>A