Canonical Allele Identifier: PA2826067602
Gene: SATB2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165988.1:p.Val323Ile
CA2045981
NM_001172517.1:c.967G>A