Canonical Allele Identifier: PA2741968998
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2688621
ClinVar RCV Id: RCV003492918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Ser1290Asn
CA346075535
NM_018263.6:c.3869G>A