Canonical Allele Identifier: PA645477787
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 288830
ClinVar RCV Id: RCV000370944 RCV002518057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Cys1717Tyr
CA10606239
NM_001130987.2:c.5150G>A