Canonical Allele Identifier: PA645477601
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 6677
ClinVar RCV Id: RCV000007064
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Asp643Tyr
CA253909
NM_001130987.2:c.1927G>T