Canonical Allele Identifier: PA180452
Gene: SOX3 HGNC NCBI

Linked Data

ClinVar Variation Id: 167718
ClinVar RCV Id: RCV000153990 RCV000454344 RCV000878811 RCV000720991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005625.2:p.Val53Leu
CA180451
NM_005634.3:c.157G>C
CA414479366
NM_005634.3:c.157G>T