Canonical Allele Identifier: PA2573082491
Gene: SOX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1303152
ClinVar RCV Id: RCV001756651

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003097.1:p.His101Arg
CA355473574
NM_003106.4:c.302A>G