Canonical Allele Identifier: PA658670016
Gene: SOX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 449939
ClinVar RCV Id: RCV000520284

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003097.1:p.Arg43Trp
CA355473179
NM_003106.4:c.127C>T