Canonical Allele Identifier: PA2828108081
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1537526
ClinVar RCV Id: RCV002166990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Thr1311Ser
CA9808967
NM_001363734.1:c.3932C>G
CA408564475
NM_001363734.1:c.3931A>T