Canonical Allele Identifier: PA2828319262
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2552510
ClinVar RCV Id: RCV003287853

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356276.1:p.Glu1129Lys
CA1557350
NM_001369347.1:c.3385G>A