Canonical Allele Identifier: PA645477615
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 290178
ClinVar RCV Id: RCV000304844 RCV000804560 RCV000726444 RCV001279899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124459.1:p.Thr720Met
CA1706069
NM_001130987.2:c.2159C>T