Allele Registry

Canonical Allele Identifier: PA2825770837

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000533199

RCV001755866

RCV001834801

ClinVar Variation:

471324

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124458.1:p.Arg2031Trp	CA1707654 NM_001130986.2:c.6091C>T