Allele Registry

Canonical Allele Identifier: PA2573263441

Gene: ASXL1 HGNC NCBI

ClinVar Variation Id: 1679780

HGVS (amino-acid)	Matching Registered Transcripts
NP_056153.2:p.Phe1305Leu	CA408564059 NM_015338.6:c.3913T>C CA408564062 NM_015338.6:c.3915T>A CA408564063 NM_015338.6:c.3915T>G