Allele Registry

Canonical Allele Identifier: PA2825692832

Gene: DYSF HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000080277

RCV000210633

RCV000499917

RCV000527027

RCV000675166

RCV001449935

RCV001573049

RCV003891555

RCV003993796

ClinVar Variation:

94311

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123927.1:p.Gly129Glu	CA147747 NM_001130455.2:c.386G>A