Canonical Allele Identifier: PA2573263359
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1378558
ClinVar RCV Id: RCV001881203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Asp1180Gly
CA9808848
NM_015338.6:c.3539A>G