Canonical Allele Identifier: PA2825769280
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_001124458.1:p.Asp612Tyr
CA253909
NM_001130986.2:c.1834G>T