Canonical Allele Identifier: PA2828107935
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2428393
ClinVar RCV Id: RCV003120004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Ala1064Val
CA408562924
NM_001363734.1:c.3191C>T