Canonical Allele Identifier: PA1139718233
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 915461
ClinVar RCV Id: RCV001170070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Trp142Ser
CA411499989
NM_006941.4:c.425G>C