Canonical Allele Identifier: PA2825748950
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 896081
ClinVar RCV Id: RCV001138530
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Leu2061Val
CA347227885
NM_001130976.2:c.6181C>G