Canonical Allele Identifier: PA2580423057
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2055420
ClinVar RCV Id: RCV002947243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Thr1396Met
CA1557341
NM_018263.6:c.4187C>T