Canonical Allele Identifier: PA2828107911
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2973389
ClinVar RCV Id: RCV003830483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Arg1029Gly
CA408562704
NM_001363734.1:c.3085A>G