Canonical Allele Identifier: PA2827476836
Gene: SCN11A HGNC NCBI

Linked Data

ClinVar Variation Id: 541583
ClinVar RCV Id: RCV000651888 RCV002343375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336182.1:p.Ile1739Val
CA2321374
NM_001349253.2:c.5215A>G