Canonical Allele Identifier: PA645477516
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 167016
ClinVar RCV Id: RCV000153173 RCV001140455
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Ala202Val
CA179983
NM_001130987.2:c.605C>T