Canonical Allele Identifier: PA2828318937
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2138514
ClinVar RCV Id: RCV003041434

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356275.1:p.Ile1224Phe
CA1557416
NM_001369346.1:c.3670A>T