Canonical Allele Identifier: PA2828108050
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1506052
ClinVar RCV Id: RCV002035900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Arg1255His
CA9808930
NM_001363734.1:c.3764G>A