Canonical Allele Identifier: PA645430881
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 229266
ClinVar RCV Id: RCV000214833 RCV000660274 RCV001420589 RCV001544623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Cys71Gly
CA10228708
NM_006941.4:c.211T>G