Canonical Allele Identifier: PA2827789617
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68562
ClinVar RCV Id: RCV000059437
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Phe1658Ser
CA266092
NM_001353960.2:c.4973T>C