Canonical Allele Identifier: PA2741934538
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2836702
ClinVar RCV Id: RCV003690222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Ala110Thr
CA411500624
NM_006941.4:c.328G>A