Allele Registry

Canonical Allele Identifier: PA2825768019

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 94324

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124457.1:p.Lys1498Thr	CA222170 NM_001130985.2:c.4493A>C