Allele Registry

Canonical Allele Identifier: PA2825764959

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000385438

RCV000525552

RCV001535516

ClinVar Variation:

288008

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124456.1:p.Ala770Val	CA1706139 NM_001130984.2:c.2309C>T