Canonical Allele Identifier: PA658829113
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 547781
ClinVar RCV Id: RCV000660281
ClinVar Variation Id: 801016
ClinVar RCV Id: RCV000985243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Trp142Cys
CA411499984
NM_006941.4:c.426G>T
CA411499986
NM_006941.4:c.426G>C