Canonical Allele Identifier: PA2741951012
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2913260
ClinVar RCV Id: RCV003738813

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Ala1290Val
CA9808919
NM_015338.6:c.3869C>T