Canonical Allele Identifier: PA1139718191
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 995931
ClinVar RCV Id: RCV001290169
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Met112Arg
CA411500558
NM_006941.4:c.335T>G