Canonical Allele Identifier: PA2580337896
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2195342
ClinVar RCV Id: RCV002647652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Gly317Ser
CA411492515
NM_006941.4:c.949G>A