Canonical Allele Identifier: PA2828318981
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_001356275.1:p.Thr1338Met
CA1557341
NM_001369346.1:c.4013C>T