Canonical Allele Identifier: PA2828108075
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1969637
ClinVar RCV Id: RCV002717282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.His1300Arg
CA408564401
NM_001363734.1:c.3899A>G