Canonical Allele Identifier: PA2828318927
Gene: ASXL2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3062134
ClinVar RCV Id: RCV003985244

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356275.1:p.Ala1204Ser
CA346076095
NM_001369346.1:c.3610G>T