Canonical Allele Identifier: PA2573252286
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1353113
ClinVar RCV Id: RCV001869917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Pro398Leu
CA324160734
NM_006941.4:c.1193C>T