Canonical Allele Identifier: PA2741899949
Gene: SOX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2577750
ClinVar RCV Id: RCV003325087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003097.1:p.Gly54Trp
CA355473257
NM_003106.4:c.160G>T