Canonical Allele Identifier: PA2828107953
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2193552
ClinVar RCV Id: RCV002623990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Gly1089Val
CA9808829
NM_001363734.1:c.3266G>T