Canonical Allele Identifier: PA2573263456
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1352630
ClinVar RCV Id: RCV002049510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Pro1317Thr
CA313926368
NM_015338.6:c.3949C>A