Canonical Allele Identifier: PA658659285
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 461265
ClinVar RCV Id: RCV000540121
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Trp1219Arg
CA349055964
NM_001165963.4:c.3655T>C
CA349055968
NM_001165963.4:c.3655T>A