Canonical Allele Identifier: PA645477636
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 195961
ClinVar RCV Id: RCV000176653 RCV000553449 RCV001267331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Val909Ile
CA242686
NM_001130987.2:c.2725G>A