Canonical Allele Identifier: PA2829679029
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 3167697
ClinVar RCV Id: RCV004457541
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Pro91Ser
CA411501187
NM_006941.4:c.271C>T