Canonical Allele Identifier: PA2828108051
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1352630
ClinVar RCV Id: RCV002049510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Pro1256Thr
CA313926368
NM_001363734.1:c.3766C>A