Canonical Allele Identifier: PA2580393795
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2428393
ClinVar RCV Id: RCV003120004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Ala1125Val
CA408562924
NM_015338.6:c.3374C>T