Canonical Allele Identifier: PA2825693627
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 6677
ClinVar RCV Id: RCV000007064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123927.1:p.Asp626Tyr
CA253909
NM_001130455.2:c.1876G>T