Canonical Allele Identifier: PA2825770109
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 1932275
ClinVar RCV Id: RCV002649399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124458.1:p.Asn1360Lys
CA49779104
NM_001130986.2:c.4080C>A
CA347228694
NM_001130986.2:c.4080C>G