Canonical Allele Identifier: PA2828319223
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1383623

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356276.1:p.Arg1023His
CA1557413
NM_001369347.1:c.3068G>A