Canonical Allele Identifier: PA2825695667
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_001123927.1:p.Val1841Met
CA10604806
NM_001130455.2:c.5521G>A