Canonical Allele Identifier: PA2741899959
Gene: SOX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2545055
ClinVar RCV Id: RCV003257359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003097.1:p.Met102Ile
CA355473584
NM_003106.4:c.306G>T
CA355473585
NM_003106.4:c.306G>C
CA355473586
NM_003106.4:c.306G>A