Canonical Allele Identifier: PA2828107907
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1283377
ClinVar RCV Id: RCV001696521 RCV002260355 RCV002538621
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Ser1018Pro
CA9808783
NM_001363734.1:c.3052T>C