Canonical Allele Identifier: PA2828108057
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2815622
ClinVar RCV Id: RCV003685512

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Met1262Ile
CA408564166
NM_001363734.1:c.3786G>A
CA408564167
NM_001363734.1:c.3786G>C
CA408564168
NM_001363734.1:c.3786G>T