Canonical Allele Identifier: PA915973852
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 565765
ClinVar RCV Id: RCV000685404 RCV001276437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124454.1:p.Glu1053Val
CA347216949
NM_001130982.2:c.3158A>T