Allele Registry

Canonical Allele Identifier: PA2828107892

Gene: ASXL1 HGNC NCBI

ClinVar RCV:

RCV000171345

ClinVar Variation:

191161

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350663.1:p.Glu936Gln	CA236147 NM_001363734.1:c.2806G>C