Canonical Allele Identifier: PA236146
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 191160

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Ser151Arg
CA236144
NM_015338.6:c.453C>A
CA408552082
NM_015338.6:c.451A>C
CA408552095
NM_015338.6:c.453C>G