Canonical Allele Identifier: PA2825769839
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 282705
ClinVar RCV Id: RCV000284503 RCV000648010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124458.1:p.Val1106Met
CA1706555
NM_001130986.2:c.3316G>A