Allele Registry

Canonical Allele Identifier: PA2825765679

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000313317

RCV000370350

RCV000517870

RCV000727268

RCV001083961

RCV001274832

ClinVar Variation:

336971

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124456.1:p.Pro1387Ala	CA1706942 NM_001130984.2:c.4159C>G