Canonical Allele Identifier: PA156995
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133580

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Met1249Val
CA156993
NM_015338.6:c.3745A>G
CA2580612057
NM_015338.6:c.3745_3759delinsGTGTCACAGGACAGC