Canonical Allele Identifier: PA915973941
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_001124454.1:p.Val1151Met
CA1706555
NM_001130982.2:c.3451G>A