Canonical Allele Identifier: PA2825770009
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 284252
ClinVar RCV Id: RCV000316493 RCV001855139
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124458.1:p.Leu1257Arg
CA10604735
NM_001130986.2:c.3770T>G