Canonical Allele Identifier: PA645477608
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 290745
ClinVar RCV Id: RCV000288710 RCV000311911 RCV000383412 RCV001139894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Gly698Val
CA1706038
NM_001130987.2:c.2093G>T