Canonical Allele Identifier: PA2580337853
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2436253
ClinVar RCV Id: RCV003138590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Asn109Lys
CA411500629
NM_006941.4:c.327C>G
CA411500636
NM_006941.4:c.327C>A