Canonical Allele Identifier: PA1139736063
Gene: SCN11A HGNC NCBI

Linked Data

ClinVar Variation Id: 938736
ClinVar RCV Id: RCV001208014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054858.2:p.Arg1745Gln
CA2321366
NM_014139.3:c.5234G>A