Canonical Allele Identifier: PA658818602
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 488043
ClinVar RCV Id: RCV000626402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Ser135Arg
CA411500118
NM_006941.4:c.405C>G
CA411500119
NM_006941.4:c.405C>A
CA411500124
NM_006941.4:c.403A>C