Canonical Allele Identifier: PA2829468873
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2885593
ClinVar RCV Id: RCV003735522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003485.1:p.Asp1837His
CA347223076
NM_003494.4:c.5509G>C