Canonical Allele Identifier: PA2827475976
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_001336182.1:p.Arg838Gln
CA2322027
NM_001349253.2:c.2513G>A