Canonical Allele Identifier: PA2827781178
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 893876
ClinVar RCV Id: RCV001133024 RCV001133023
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Asn1955Lys
CA349063275
NM_001353955.2:c.5865C>G
CA349063276
NM_001353955.2:c.5865C>A