Canonical Allele Identifier: PA209304
Gene: ASXL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 210368

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_085135.1:p.Pro642Leu
CA209303
NM_030632.1:c.1925C>T