Canonical Allele Identifier: PA645428810
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 377157
ClinVar RCV Id: RCV000428840 RCV002480279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Gln1371Lys
CA1557360
NM_018263.6:c.4111C>A