Allele Registry

Canonical Allele Identifier: PA111165

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000538326

ClinVar Variation:

471280

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Trp52Arg	CA347216250 NM_003494.4:c.154T>A CA347216252 NM_003494.4:c.154T>C