Canonical Allele Identifier: PA2826067309
Gene: SATB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2419641
ClinVar RCV Id: RCV003115526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165988.1:p.Gln36His
CA350388469
NM_001172517.1:c.108G>T
CA350388470
NM_001172517.1:c.108G>C