Canonical Allele Identifier: PA645430879
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 229265
ClinVar RCV Id: RCV000221276 RCV001509097
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Asp64Val
CA10228717
NM_006941.4:c.191A>T