Canonical Allele Identifier: PA2825754936
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 336969
ClinVar RCV Id: RCV000291639 RCV000419423 RCV001272842 RCV000346595 RCV001753802 RCV001080538
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124451.1:p.Ile1356Val
CA1706842
NM_001130979.2:c.4066A>G