Canonical Allele Identifier: PA2573273953
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1384509
ClinVar RCV Id: RCV001924849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Met1273Ile
CA346075842
NM_018263.6:c.3819G>T
CA346075845
NM_018263.6:c.3819G>C
CA346075847
NM_018263.6:c.3819G>A