Canonical Allele Identifier: PA2828319219
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1722442
ClinVar RCV Id: RCV002302556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356276.1:p.Lys1020Met
CA346075709
NM_001369347.1:c.3059A>T