Canonical Allele Identifier: PA2827475551
Gene: SCN11A HGNC NCBI

Linked Data

ClinVar Variation Id: 1434851
ClinVar RCV Id: RCV001962558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336182.1:p.Leu374Phe
CA352168330
NM_001349253.2:c.1120C>T