Allele Registry

Canonical Allele Identifier: PA2825770619

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000648015

RCV001276864

RCV002222581

RCV003144430

ClinVar Variation:

538643

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124458.1:p.Thr1818Met	CA1707445 NM_001130986.2:c.5453C>T