Allele Registry

Canonical Allele Identifier: PA256564

Gene: SOX2 HGNC NCBI

ClinVar Allele:

27856

ClinVar RCV:

RCV000013665

ClinVar Variation:

12817

HGVS (amino-acid)	Matching Registered Transcripts
NP_003097.1:p.Leu97Pro	CA256562 NM_003106.4:c.290T>C