Canonical Allele Identifier: PA915988013
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 767431

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Glu359Asp
CA10228536
NM_006941.4:c.1077G>C
CA411491173
NM_006941.4:c.1077G>T