Canonical Allele Identifier: PA645492306
Gene: ASXL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 402202

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_085135.1:p.Gly1046Arg
CA8934033
NM_030632.1:c.3136G>A
CA402184528
NM_030632.1:c.3136G>C