Canonical Allele Identifier: PA2580423045
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2231804
ClinVar RCV Id: RCV002708262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Val1277Leu
CA346075774
NM_018263.6:c.3829G>T
CA346075777
NM_018263.6:c.3829G>C