Canonical Allele Identifier: PA2499275441
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1194338

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Asn304Ser
CA10228569
NM_006941.4:c.911A>G