Canonical Allele Identifier: PA2825768018
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2829309
ClinVar RCV Id: RCV003735245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124457.1:p.Lys1498Ile
CA347217870
NM_001130985.2:c.4493A>T