Canonical Allele Identifier: PA2828318968
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_001356275.1:p.Gln1313Lys
CA1557360
NM_001369346.1:c.3937C>A