Canonical Allele Identifier: PA2828318938
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2427929
ClinVar RCV Id: RCV003116900 RCV003140249 RCV004245952
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356275.1:p.Arg1225Cys
CA1557415
NM_001369346.1:c.3673C>T