Canonical Allele Identifier: PA658807266
Gene: SCN11A HGNC NCBI

Linked Data

ClinVar Variation Id: 541570
ClinVar RCV Id: RCV000651875 RCV001566282 RCV002440365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054858.2:p.Arg838Gln
CA2322027
NM_014139.3:c.2513G>A