Canonical Allele Identifier: PA2580423048
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2427929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Arg1283Cys
CA1557415
NM_018263.6:c.3847C>T