Allele Registry

Canonical Allele Identifier: PA2825757776

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000265900

RCV001859602

RCV003401247

ClinVar Variation:

284471

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124452.1:p.Val1857Met	CA10604806 NM_001130980.2:c.5569G>A