Canonical Allele Identifier: PA2825769282
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 1504301
ClinVar RCV Id: RCV002047764 RCV003146477
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124458.1:p.Met613Val
CA1705982
NM_001130986.2:c.1837A>G