Canonical Allele Identifier: PA658829112
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 547779
ClinVar RCV Id: RCV000660279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Leu122Val
CA411500332
NM_006941.4:c.364C>G