Canonical Allele Identifier: PA2573252213
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1506349
ClinVar RCV Id: RCV002006662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Asp64Ala
CA10228719
NM_006941.4:c.191A>C