Canonical Allele Identifier: PA2828318985
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 449235
ClinVar RCV Id: RCV000522632

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356275.1:p.Cys1352Gly
CA346073615
NM_001369346.1:c.4054T>G