Canonical Allele Identifier: PA2573091812
Gene: ASXL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1316385
ClinVar RCV Id: RCV001766291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056153.2:p.Pro1360Leu
CA9808959
NM_015338.6:c.4079C>T