Canonical Allele Identifier: PA2499275445
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1027697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Gly389Ser
CA411490320
NM_006941.4:c.1165G>A