Canonical Allele Identifier: PA2827476831
Gene: SCN11A HGNC NCBI

Linked Data

ClinVar Variation Id: 474745
ClinVar RCV Id: RCV000540407 RCV001653919 RCV002341454 RCV003962591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336182.1:p.Gly1736Val
CA2321375
NM_001349253.2:c.5207G>T