Allele Registry

Canonical Allele Identifier: PA2826067623

Gene: SATB2 HGNC NCBI

ClinVar Allele:

1112095

ClinVar RCV:

RCV001454933

ClinVar Variation:

1123789

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165988.1:p.Asn355Thr	CA350387376 NM_001172517.1:c.1064A>C