Canonical Allele Identifier: PA2580337899
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1953291
ClinVar RCV Id: RCV002681756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.His387Gln
CA10228517
NM_006941.4:c.1161C>G
CA411490357
NM_006941.4:c.1161C>A