Canonical Allele Identifier: PA2741991350
Gene: ASXL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2504439
ClinVar RCV Id: RCV003231900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_085135.1:p.Ser1520Phe
CA297793668
NM_030632.1:c.4559C>T