Canonical Allele Identifier: PA2580393787
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2016224
ClinVar RCV Id: RCV002843790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Glu1102Gly
CA408562782
NM_015338.6:c.3305A>G