Canonical Allele Identifier: PA2580337887
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2307320
ClinVar RCV Id: RCV002900685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.His211Gln
CA411497317
NM_006941.4:c.633C>A
CA411497319
NM_006941.4:c.633C>G