Canonical Allele Identifier: PA2828108044
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Ala1251Val
CA157017
NM_001363734.1:c.3752C>T