Canonical Allele Identifier: PA2829904837
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3130605
ClinVar RCV Id: RCV004423002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Asp1257Gly
CA1557423
NM_018263.6:c.3770A>G