Canonical Allele Identifier: PA1139718171
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 902511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Phe68Leu
CA10228714
NM_006941.4:c.204C>A
CA411501521
NM_006941.4:c.204C>G
CA411501535
NM_006941.4:c.202T>C