Canonical Allele Identifier: PA645477705
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 289774
ClinVar RCV Id: RCV000266054 RCV002518100
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Val1376Met
CA1706898
NM_001130987.2:c.4126G>A