Canonical Allele Identifier: PA658818615
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 521356
ClinVar RCV Id: RCV000623200 RCV001290177 RCV002291283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Pro175Ser
CA411497800
NM_006941.4:c.523C>T