Canonical Allele Identifier: PA2580337848
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2009414
ClinVar RCV Id: RCV002838390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Val94Ala
CA411501131
NM_006941.4:c.281T>C