Canonical Allele Identifier: PA2580282543
Gene: SOX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2331236
ClinVar RCV Id: RCV002935465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003097.1:p.Leu314Val
CA355474987
NM_003106.4:c.940C>G