Canonical Allele Identifier: PA2828107901
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1695014
ClinVar RCV Id: RCV002263264

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Val1008Ile
CA9808776
NM_001363734.1:c.3022G>A