Allele Registry

Canonical Allele Identifier: PA2825748112

Gene: DYSF HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

21706

ClinVar RCV:

RCV000007049

RCV000153183

RCV000509353

RCV000658868

RCV000681611

RCV001563901

RCV004547461

ClinVar Variation:

6667

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124448.1:p.Ile1284Val	CA179991 NM_001130976.2:c.3850A>G