Canonical Allele Identifier: PA2825768769
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 284579
ClinVar RCV Id: RCV000415918 RCV000675087 RCV001844111 RCV002521923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124458.1:p.Pro135Leu
CA1705344
NM_001130986.2:c.404C>T