Canonical Allele Identifier: PA2741941238
Gene: SCN11A HGNC NCBI

Linked Data

ClinVar Variation Id: 2576562
ClinVar RCV Id: RCV003322677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054858.2:p.Arg222Ser
CA352173334
NM_014139.3:c.664C>A