Canonical Allele Identifier: PA916036471
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189992
ClinVar RCV Id: RCV000180948
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Cys968Phe
CA303499
NM_001353948.2:c.2903G>T