Canonical Allele Identifier: PA209345
Gene: ASXL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 210365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_085135.1:p.Asn485Ser
CA209344
NM_030632.1:c.1454A>G