Allele Registry

Canonical Allele Identifier: PA645477606

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000292466

RCV000328757

RCV000487642

RCV001085988

RCV001563948

RCV001563949

RCV001563950

RCV003416078

ClinVar Variation:

195598

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.Lys674Glu	CA242074 NM_001130987.2:c.2020A>G