Canonical Allele Identifier: PA2499275437
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1027698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Gly61Ser
CA324166571
NM_006941.4:c.181G>A