Canonical Allele Identifier: PA2741899988
Gene: SOX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2515667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003097.1:p.Pro264Thr
CA355474655
NM_003106.4:c.790C>A