Canonical Allele Identifier: PA2828318943
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2227716
ClinVar RCV Id: RCV002702526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356275.1:p.Ala1240Pro
CA346075405
NM_001369346.1:c.3718G>C