Canonical Allele Identifier: PA645430605
Gene: SOX11 HGNC NCBI

Linked Data

ClinVar Variation Id: 420790
ClinVar RCV Id: RCV000483495
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003099.1:p.Arg64Gly
CA16617743
NM_003108.4:c.190C>G