Canonical Allele Identifier: PA2827785969
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2153965
ClinVar RCV Id: RCV003069036

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Leu1271Ser
CA1942866
NM_001353958.2:c.3812T>C