Canonical Allele Identifier: PA2580423047
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2138514
ClinVar RCV Id: RCV003041434
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Ile1282Phe
CA1557416
NM_018263.6:c.3844A>T