Canonical Allele Identifier: PA111686
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 7397
ClinVar RCV Id: RCV000007821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Ser135Thr
CA118757
NM_006941.4:c.404G>C