Canonical Allele Identifier: PA2826066691
Gene: SATB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2419641
ClinVar RCV Id: RCV003115526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165980.1:p.Gln36His
CA350388469
NM_001172509.2:c.108G>T
CA350388470
NM_001172509.2:c.108G>C