Canonical Allele Identifier: PA2499275443
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1188631
ClinVar RCV Id: RCV001548477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Gln364Pro
CA10228527
NM_006941.4:c.1091A>C