Canonical Allele Identifier: PA2828108035
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2794032
ClinVar RCV Id: RCV003672592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Asn1235Lys
CA9808920
NM_001363734.1:c.3705T>A
CA408564007
NM_001363734.1:c.3705T>G