Canonical Allele Identifier: PA2499291878
Gene: ASXL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1257808
ClinVar RCV Id: RCV001665771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_085135.1:p.Ile1285Leu
CA8934130
NM_030632.1:c.3853A>C