Canonical Allele Identifier: PA2741899952
Gene: SOX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2634342
ClinVar RCV Id: RCV004552519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003097.1:p.Leu81Phe
CA355473446
NM_003106.4:c.241C>T