Canonical Allele Identifier: PA2828107930
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2879233
ClinVar RCV Id: RCV003710588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Lys1059Asn
CA408562898
NM_001363734.1:c.3177G>C
CA408562899
NM_001363734.1:c.3177G>T