Canonical Allele Identifier: PA2826014066
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1685088
ClinVar RCV Id: RCV002248180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Pro1816Leu
CA349065582
NM_001165964.3:c.5447C>T