Canonical Allele Identifier: PA2580282532
Gene: SOX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2077953
ClinVar RCV Id: RCV002988385
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003097.1:p.Gly234Ser
CA355474466
NM_003106.4:c.700G>A