Canonical Allele Identifier: PA1139722084
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 982935
ClinVar RCV Id: RCV001262671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Gln1142Arg
CA408563037
NM_015338.6:c.3425A>G