Canonical Allele Identifier: PA157004
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Arg1148Cys
CA157002
NM_015338.6:c.3442C>T