Canonical Allele Identifier: PA2828107913
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1985398
ClinVar RCV Id: RCV002800520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Ala1030Thr
CA408562711
NM_001363734.1:c.3088G>A