Canonical Allele Identifier: PA2828107989
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2168558
ClinVar RCV Id: RCV003082632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Ile1159Phe
CA9808871
NM_001363734.1:c.3475A>T