Canonical Allele Identifier: PA2825749089
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 970142
ClinVar RCV Id: RCV001245659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124449.1:p.Ala129Thr
CA347205451
NM_001130977.2:c.385G>A