Canonical Allele Identifier: PA2741969021
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2780003
ClinVar RCV Id: RCV003665461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Lys1411Arg
CA346073603
NM_018263.6:c.4232A>G