Canonical Allele Identifier: PA1139718375
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 982663
ClinVar RCV Id: RCV001262265 RCV002537632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Ala361Thr
CA10228533
NM_006941.4:c.1081G>A