Allele Registry

Canonical Allele Identifier: PA2826066956

Gene: SATB2 HGNC NCBI

ClinVar RCV:

RCV001454933

ClinVar Variation:

1123789

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165980.1:p.Asn355Thr	CA350387376 NM_001172509.2:c.1064A>C