Allele Registry

Canonical Allele Identifier: PA2829467786

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000331066

RCV000820404

RCV001828229

ClinVar Variation:

286443

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Thr1365Met	CA1706904 NM_003494.4:c.4094C>T