Canonical Allele Identifier: PA658806966
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 497674
ClinVar RCV Id: RCV000592288 RCV001867926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Tyr1687Cys
CA347220291
NM_001130987.2:c.5060A>G