Canonical Allele Identifier: PA2826066688
Gene: SATB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1001127
ClinVar RCV Id: RCV001297369
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165980.1:p.Ala32Thr
CA350388499
NM_001172509.2:c.94G>A