Allele Registry

Canonical Allele Identifier: PA2829465697

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000536797

RCV000711545

RCV001835762

ClinVar Variation:

289471

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Val42Met	CA1705230 NM_003494.4:c.124G>A