Allele Registry

Canonical Allele Identifier: PA2826066907

Gene: SATB2 HGNC NCBI

ClinVar RCV:

RCV001891527

ClinVar Variation:

1396001

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165980.1:p.Pro287Ser	CA2045995 NM_001172509.2:c.859C>T