Canonical Allele Identifier: PA2828319247
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2066896
ClinVar RCV Id: RCV002943631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356276.1:p.Gln1089His
CA1557372
NM_001369347.1:c.3267G>T
CA1557373
NM_001369347.1:c.3267G>C