Canonical Allele Identifier: PA2580282705
Gene: SOX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2302212
ClinVar RCV Id: RCV002850770
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003099.1:p.Lys88Glu
CA345866316
NM_003108.4:c.262A>G