Canonical Allele Identifier: PA2828318945
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2608912
ClinVar RCV Id: RCV003357908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356275.1:p.Thr1244Ala
CA346075329
NM_001369346.1:c.3730A>G