Canonical Allele Identifier: PA2573273967
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1479143
ClinVar RCV Id: RCV001976636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Met1339Val
CA1557378
NM_018263.6:c.4015A>G