Canonical Allele Identifier: PA2580337869
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1878656
ClinVar RCV Id: RCV002510747

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Ser135Ile
CA411500120
NM_006941.4:c.404G>T
CA2580099764
NM_006941.4:c.404_405delinsTT