Canonical Allele Identifier: PA2580337900
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1695045
ClinVar RCV Id: RCV002263295

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Arg397His
CA10228514
NM_006941.4:c.1190G>A