Canonical Allele Identifier: PA2827787701
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189864
ClinVar RCV Id: RCV000180817 RCV000329798 RCV001377988
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Asn359Ser
CA303143
NM_001353960.2:c.1076A>G