Canonical Allele Identifier: PA2580423043
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2138515
ClinVar RCV Id: RCV003050599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Gln1272His
CA1557419
NM_018263.6:c.3816G>T
CA346075873
NM_018263.6:c.3816G>C