Allele Registry

Canonical Allele Identifier: PA2828318968

Gene: ASXL2 HGNC NCBI

ClinVar RCV:

RCV000428840

RCV002480279

ClinVar Variation:

377157

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356275.1:p.Gln1313Lys	CA1557360 NM_001369346.1:c.3937C>A