Canonical Allele Identifier: PA2828319272
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1703089
ClinVar RCV Id: RCV002280212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356276.1:p.Gly1152Arg
CA346073597
NM_001369347.1:c.3454G>C