Canonical Allele Identifier: PA2741951023
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2905612
ClinVar RCV Id: RCV003731789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Pro1340Thr
CA9808948
NM_015338.6:c.4018C>A