Canonical Allele Identifier: PA2741969001
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2613394
ClinVar RCV Id: RCV003362326 RCV003778050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Pro1314Leu
CA1557393
NM_018263.6:c.3941C>T