Canonical Allele Identifier: PA111615
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 7410
ClinVar RCV Id: RCV000007835
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Gln174Pro
CA118782
NM_006941.4:c.521A>C