ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA122733
Gene: SOX2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000013674
RCV000624040
RCV002513019
ClinVar Variation:
12826
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003097.1:p.Ala191Thr
CA122731
NM_003106.4:c.571G>A