Canonical Allele Identifier: PA2580472161
Gene: ASXL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2272278
ClinVar RCV Id: RCV002799722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_085135.1:p.Asn485Thr
CA402175381
NM_030632.1:c.1454A>C