Canonical Allele Identifier: PA2828318987
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2780003
ClinVar RCV Id: RCV003665461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356275.1:p.Lys1353Arg
CA346073603
NM_001369346.1:c.4058A>G