Canonical Allele Identifier: PA2573263316
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1356676
ClinVar RCV Id: RCV001870214

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Val1108Gly
CA408562819
NM_015338.6:c.3323T>G