Canonical Allele Identifier: PA1139716502
Gene: SOX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 870447
ClinVar RCV Id: RCV001090007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003097.1:p.Thr7Met
CA355472959
NM_003106.4:c.20C>T