Canonical Allele Identifier: PA2825748194
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 864337
ClinVar RCV Id: RCV001071496
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Phe1366Ser
CA347228816
NM_001130976.2:c.4097T>C