Canonical Allele Identifier: PA645430891
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 229267
ClinVar RCV Id: RCV000217827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Lys105Gln
CA10577153
NM_006941.4:c.313A>C