Canonical Allele Identifier: PA2828318957
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1464930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356275.1:p.Ser1276Ala
CA1557380
NM_001369346.1:c.3826T>G