Canonical Allele Identifier: PA915987976
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 809363
ClinVar RCV Id: RCV000997922

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Ala110Val
CA411500596
NM_006941.4:c.329C>T