Canonical Allele Identifier: PA2825771115
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2102928
ClinVar RCV Id: RCV003037820
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Leu560Val
CA347217508
NM_001130987.2:c.1678C>G