Canonical Allele Identifier: PA2826067306
Gene: SATB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1001127
ClinVar RCV Id: RCV001297369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165988.1:p.Ala32Thr
CA350388499
NM_001172517.1:c.94G>A