Allele Registry

Canonical Allele Identifier: PA236149

Gene: ASXL1 HGNC NCBI

ClinVar RCV:

RCV000171345

ClinVar Variation:

191161

HGVS (amino-acid)	Matching Registered Transcripts
NP_056153.2:p.Glu997Gln	CA236147 NM_015338.6:c.2989G>C