Canonical Allele Identifier: PA2828107918
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1675100
ClinVar RCV Id: RCV002204531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Val1040Glu
CA408562775
NM_001363734.1:c.3119T>A