Canonical Allele Identifier: PA2828107944
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2963784
ClinVar RCV Id: RCV003825422

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Thr1078Arg
CA408563015
NM_001363734.1:c.3233C>G