Canonical Allele Identifier: PA2580282531
Gene: SOX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2331561
ClinVar RCV Id: RCV002917062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003097.1:p.Pro221Arg
CA355474384
NM_003106.4:c.662C>G