Canonical Allele Identifier: PA2741951021
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2632627
ClinVar RCV Id: RCV004550796
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Pro1330Arg
CA408564208
NM_015338.6:c.3989C>G