Allele Registry

Canonical Allele Identifier: PA110903

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000301411

RCV001082288

RCV001833344

RCV003091891

ClinVar Variation:

285148

2166693

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Gly155Arg	CA1705380 NM_003494.4:c.463G>A CA49758528 NM_003494.4:c.463G>C