Canonical Allele Identifier: PA2828108059
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2188044
ClinVar RCV Id: RCV002616226
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Pro1265Arg
CA9808938
NM_001363734.1:c.3794C>G