Canonical Allele Identifier: PA2828108078
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1335459
ClinVar RCV Id: RCV001816304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Val1306Ile
CA9808964
NM_001363734.1:c.3916G>A