Canonical Allele Identifier: PA2573082492
Gene: SOX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1313635
ClinVar RCV Id: RCV001763999
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003097.1:p.Pro112Thr
CA355473654
NM_003106.4:c.334C>A