Canonical Allele Identifier: PA2580337850
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2127667
ClinVar RCV Id: RCV003055612
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Ser98Arg
CA411500992
NM_006941.4:c.294C>G
CA411500996
NM_006941.4:c.294C>A
CA411501014
NM_006941.4:c.292A>C