Canonical Allele Identifier: PA2827780561
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12895
ClinVar RCV Id: RCV000013756 RCV000013757
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Val1599Phe
CA256614
NM_001353955.2:c.4795G>T