Canonical Allele Identifier: PA111586
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2138446
ClinVar RCV Id: RCV003064655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Arg106Trp
CA411500741
NM_006941.4:c.316C>T