Canonical Allele Identifier: PA2828319237
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1376565
ClinVar RCV Id: RCV001885989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356276.1:p.Pro1065Arg
CA1557385
NM_001369347.1:c.3194C>G