Canonical Allele Identifier: PA2741951003
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2900877
ClinVar RCV Id: RCV003729007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Asp1230Tyr
CA9808879
NM_015338.6:c.3688G>T