Canonical Allele Identifier: PA2826066689
Gene: SATB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3157934
ClinVar RCV Id: RCV004450255
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165980.1:p.Arg33Trp
CA350388493
NM_001172509.2:c.97C>T