Canonical Allele Identifier: PA2828108048
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2166142
ClinVar RCV Id: RCV003084727

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Arg1255Cys
CA9808929
NM_001363734.1:c.3763C>T