Canonical Allele Identifier: PA157019
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Ala1312Val
CA157017
NM_015338.6:c.3935C>T