Canonical Allele Identifier: PA2580337843
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1709423

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Val92Met
CA10228701
NM_006941.4:c.274G>A