Canonical Allele Identifier: PA2825766970
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2102928
ClinVar RCV Id: RCV003037820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Leu560Val
CA347217508
NM_001130985.2:c.1678C>G