Canonical Allele Identifier: PA2828318954
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1376565
ClinVar RCV Id: RCV001885989
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356275.1:p.Pro1267Arg
CA1557385
NM_001369346.1:c.3800C>G