Canonical Allele Identifier: PA2573273962
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1376565
ClinVar RCV Id: RCV001885989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060733.4:p.Pro1325Arg
CA1557385
NM_018263.6:c.3974C>G