Canonical Allele Identifier: PA2828318934
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2231804
ClinVar RCV Id: RCV002708262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356275.1:p.Val1219Leu
CA346075774
NM_001369346.1:c.3655G>T
CA346075777
NM_001369346.1:c.3655G>C