Canonical Allele Identifier: PA2828107955
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1318724
ClinVar RCV Id: RCV001768348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Ser1090Cys
CA408563087
NM_001363734.1:c.3269C>G