Canonical Allele Identifier: PA2828107905
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1212249
ClinVar RCV Id: RCV001589487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Arg1012Cys
CA9808781
NM_001363734.1:c.3034C>T