Canonical Allele Identifier: PA2580393906
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1960951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Val1349Ala
CA408564326
NM_015338.6:c.4046T>C