Canonical Allele Identifier: PA111615
Gene: SOX10 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Gln174Pro
CA118782
NM_006941.4:c.521A>C