Canonical Allele Identifier: PA2827788967
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 663255
ClinVar RCV Id: RCV000821102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Arg1290Gly
CA349053101
NM_001353960.2:c.3868A>G