Canonical Allele Identifier: PA2826067653
Gene: SATB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 427210
ClinVar RCV Id: RCV000489186

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165988.1:p.Gly392Glu
CA350386590
NM_001172517.1:c.1175G>A