Canonical Allele Identifier: PA234848
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 167638
ClinVar RCV Id: RCV000153887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Lys1270Asn
CA234845
NM_001165963.4:c.3810A>C
CA349054259
NM_001165963.4:c.3810A>T