Canonical Allele Identifier: PA2828108071
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2312238
ClinVar RCV Id: RCV002884536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Asp1294Gly
CA9808956
NM_001363734.1:c.3881A>G