Canonical Allele Identifier: PA2828107902
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2099892
ClinVar RCV Id: RCV003021945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350663.1:p.Val1008Leu
CA408562571
NM_001363734.1:c.3022G>T
CA408562572
NM_001363734.1:c.3022G>C