Canonical Allele Identifier: PA915975008
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 647886

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Ala1978Thr
CA1707553
NM_001130987.2:c.5932G>A