Canonical Allele Identifier: PA2580393871
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1902197
ClinVar RCV Id: RCV002580101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Arg1273His
CA9808912
NM_015338.6:c.3818G>A