Canonical Allele Identifier: PA2826067613
Gene: SATB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3005174
ClinVar RCV Id: RCV003868301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165988.1:p.Ile335Val
CA350387602
NM_001172517.1:c.1003A>G