Canonical Allele Identifier: PA658662909
Gene: SOX10 HGNC NCBI

Linked Data

ClinVar Variation Id: 452278
ClinVar RCV Id: RCV000519667 RCV000767097 RCV001149119 RCV001149120 RCV004541634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008872.1:p.Ala44Gly
CA10228723
NM_006941.4:c.131C>G