Canonical Allele Identifier: PA2741899978
Gene: SOX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2726288
ClinVar RCV Id: RCV003514171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003097.1:p.Met197Ile
CA355474215
NM_003106.4:c.591G>A
CA355474216
NM_003106.4:c.591G>C
CA355474217
NM_003106.4:c.591G>T