Canonical Allele Identifier: PA2825770037
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 197005
ClinVar RCV Id: RCV000177910 RCV002516759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124458.1:p.Ser1289Pro
CA244883
NM_001130986.2:c.3865T>C