Allele Registry

Canonical Allele Identifier: PA916044092

Gene: ASXL1 HGNC NCBI

ClinVar RCV:

RCV000120095

RCV002515817

ClinVar Variation:

133582

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350663.1:p.Ser967Leu	CA156999 NM_001363734.1:c.2900C>T