Canonical Allele Identifier: PA2828108062
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2982045
ClinVar RCV Id: RCV003840627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Pro1270Arg
CA408564213
NM_001363734.1:c.3809C>G