Canonical Allele Identifier: PA2828319252
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 377157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356276.1:p.Gln1111Lys
CA1557360
NM_001369347.1:c.3331C>A