Allele Registry

Canonical Allele Identifier: PA2829467482

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000382528

RCV000648004

RCV001272831

RCV003243035

ClinVar Variation:

281301

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Asp1163Asn	CA1706621 NM_003494.4:c.3487G>A