Canonical Allele Identifier: PA645505286
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 425268
ClinVar RCV Id: RCV000487846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Leu1082del
CA9808784
NM_015338.6:c.3244_3246del