Canonical Allele Identifier: PA2825765783
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 94324
ClinVar RCV Id: RCV000080290 RCV001854416 RCV003460752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124456.1:p.Lys1488Thr
CA222170
NM_001130984.2:c.4463A>C