Canonical Allele Identifier: PA2828108079
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 548554
ClinVar RCV Id: RCV000662077 RCV000662076 RCV002530591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Lys1310del
CA9808965
NM_001363734.1:c.3929_3931del