Canonical Allele Identifier: PA658818607
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 505653
ClinVar RCV Id: RCV000615378 RCV001290172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Trp142Arg
CA411500003
NM_006941.4:c.424T>C
CA411500006
NM_006941.4:c.424T>A