Canonical Allele Identifier: PA891865164
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 545013
ClinVar RCV Id: RCV000721947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Gly139Cys
CA411500057
NM_006941.4:c.415G>T