Canonical Allele Identifier: PA2825771108
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 1409880
ClinVar RCV Id: RCV001939946 RCV003146344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Glu549Gly
CA49792919
NM_001130987.2:c.1646A>G