Canonical Allele Identifier: PA2828107946
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 982935
ClinVar RCV Id: RCV001262671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Gln1081Arg
CA408563037
NM_001363734.1:c.3242A>G