Canonical Allele Identifier: PA2580423050
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2227716
ClinVar RCV Id: RCV002702526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Ala1298Pro
CA346075405
NM_018263.6:c.3892G>C