Canonical Allele Identifier: PA2828107903
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 338106
ClinVar RCV Id: RCV000361222 RCV001861163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Ala1010Val
CA9808778
NM_001363734.1:c.3029C>T