Canonical Allele Identifier: PA658818616
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 499498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Gly192Ser
CA10228651
NM_006941.4:c.574G>A