Canonical Allele Identifier: PA2828318969
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1920162
ClinVar RCV Id: RCV002591013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356275.1:p.Ala1314Gly
CA346073919
NM_001369346.1:c.3941C>G