Canonical Allele Identifier: PA2828318933
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_001356275.1:p.Val1219Ala
CA1557417
NM_001369346.1:c.3656T>C