ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825756469
Gene: DYSF
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001124452.1:p.Arg701Trp
CA1706039
NM_001130980.2:c.2101C>T