Canonical Allele Identifier: PA2741941335
Gene: SCN11A HGNC NCBI

Linked Data

ClinVar Variation Id: 2931610
ClinVar RCV Id: RCV003792632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054858.2:p.Met1674Val
CA352161697
NM_014139.3:c.5020A>G