Canonical Allele Identifier: PA2827475558
Gene: SCN11A HGNC NCBI

Linked Data

ClinVar Variation Id: 157600
ClinVar RCV Id: RCV000144935 RCV001808403 RCV002512564 RCV002460046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336182.1:p.Ile381Thr
CA171014
NM_001349253.2:c.1142T>C