Canonical Allele Identifier: PA2828107985
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2652255
ClinVar RCV Id: RCV003431286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Ser1148Asn
CA408563453
NM_001363734.1:c.3443G>A