Canonical Allele Identifier: PA2826012965
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_001159436.1:p.Trp1191Arg
CA349055964
NM_001165964.3:c.3571T>C
CA349055968
NM_001165964.3:c.3571T>A