Canonical Allele Identifier: PA2828318977
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2552510
ClinVar RCV Id: RCV003287853

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356275.1:p.Glu1331Lys
CA1557350
NM_001369346.1:c.3991G>A