Canonical Allele Identifier: PA2573089250
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1304154
ClinVar RCV Id: RCV001751921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Phe153Ile
CA411498102
NM_006941.4:c.457T>A