Canonical Allele Identifier: PA1139741888
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 975504

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Thr95Met
CA9808057
NM_001363734.1:c.284C>T