Canonical Allele Identifier: PA2825755608
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 647886

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124451.1:p.Ala1970Thr
CA1707553
NM_001130979.2:c.5908G>A