Canonical Allele Identifier: PA2741968979
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3062134
ClinVar RCV Id: RCV003985244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Ala1262Ser
CA346076095
NM_018263.6:c.3784G>T