Canonical Allele Identifier: PA645505285
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 338106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Ala1071Val
CA9808778
NM_015338.6:c.3212C>T