Canonical Allele Identifier: PA2573273964
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1464930
ClinVar RCV Id: RCV001957015 RCV003136384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Ser1334Ala
CA1557380
NM_018263.6:c.4000T>G