Canonical Allele Identifier: PA2573273972
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1354065
ClinVar RCV Id: RCV001887719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Ala1372Val
CA346073918
NM_018263.6:c.4115C>T