Canonical Allele Identifier: PA2828318984
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2861777
ClinVar RCV Id: RCV003704518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356275.1:p.Ile1350Met
CA346073624
NM_001369346.1:c.4050C>G