Canonical Allele Identifier: PA2825759650
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 94324
ClinVar RCV Id: RCV000080290 RCV001854416 RCV003460752
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124453.1:p.Lys1518Thr
CA222170
NM_001130981.2:c.4553A>C