Canonical Allele Identifier: PA2826011628
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1801093
ClinVar RCV Id: RCV002462690
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Leu224Phe
CA349074110
NM_001165964.3:c.672G>T
CA349074113
NM_001165964.3:c.672G>C