Canonical Allele Identifier: PA916064241
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 737525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Ala1386Val
CA43734177
NM_018263.6:c.4157C>T