Canonical Allele Identifier: PA2825695843
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 647886

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Ala1940Thr
CA1707553
NM_001130455.2:c.5818G>A