Canonical Allele Identifier: PA2825754124
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 1014406
ClinVar RCV Id: RCV001313136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124451.1:p.Ala627Thr
CA347218392
NM_001130979.2:c.1879G>A