Canonical Allele Identifier: PA2828318932
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1384509
ClinVar RCV Id: RCV001924849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356275.1:p.Met1215Ile
CA346075842
NM_001369346.1:c.3645G>T
CA346075845
NM_001369346.1:c.3645G>C
CA346075847
NM_001369346.1:c.3645G>A