Allele Registry

Canonical Allele Identifier: PA256573

Gene: SOX2 HGNC NCBI

ClinVar RCV:

RCV000013669

ClinVar Variation:

12821

HGVS (amino-acid)	Matching Registered Transcripts
NP_003097.1:p.Arg74Pro	CA256571 NM_003106.4:c.221G>C