Canonical Allele Identifier: PA2827777321
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68544

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Pro1439Leu
CA284961
NM_001353954.2:c.4316C>T