Canonical Allele Identifier: PA2499280971
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1283377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Ser1079Pro
CA9808783
NM_015338.6:c.3235T>C