Canonical Allele Identifier: PA2825748708
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 284471
ClinVar RCV Id: RCV000265900 RCV001859602 RCV003401247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124448.1:p.Val1826Met
CA10604806
NM_001130976.2:c.5476G>A