Canonical Allele Identifier: PA2573273955
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1383623

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Arg1283His
CA1557413
NM_018263.6:c.3848G>A