Canonical Allele Identifier: PA2580423044
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2071249
ClinVar RCV Id: RCV002949259 RCV003274108 RCV003936463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Val1277Ala
CA1557417
NM_018263.6:c.3830T>C