Canonical Allele Identifier: PA2828108067
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1960951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Val1288Ala
CA408564326
NM_001363734.1:c.3863T>C