Canonical Allele Identifier: PA645430893
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 374266
ClinVar RCV Id: RCV000415328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Arg106Gly
CA16043702
NM_006941.4:c.316C>G