Canonical Allele Identifier: PA915974132
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 289774
ClinVar RCV Id: RCV000266054 RCV002518100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124454.1:p.Val1390Met
CA1706898
NM_001130982.2:c.4168G>A