Canonical Allele Identifier: PA2580472175
Gene: ASXL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2300067
ClinVar RCV Id: RCV002878407

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_085135.1:p.Ser614Phe
CA402176515
NM_030632.1:c.1841C>T