Canonical Allele Identifier: PA2580337874
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2430605
ClinVar RCV Id: RCV003129138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Phe153Leu
CA411498089
NM_006941.4:c.459C>G
CA411498090
NM_006941.4:c.459C>A
CA411498100
NM_006941.4:c.457T>C