Canonical Allele Identifier: PA2825695639
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 538643
ClinVar RCV Id: RCV000648015 RCV001276864 RCV002222581 RCV003144430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Thr1832Met
CA1707445
NM_001130455.2:c.5495C>T