Canonical Allele Identifier: PA111649
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1065836
ClinVar RCV Id: RCV001775030
ClinVar Variation Id: 1185089
ClinVar RCV Id: RCV001822911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Met112Ile
CA411500550
NM_006941.4:c.336G>T
CA411500552
NM_006941.4:c.336G>C
CA411500554
NM_006941.4:c.336G>A