Canonical Allele Identifier: PA2826259663
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 190013
ClinVar RCV Id: RCV000180969 RCV000442784
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Ala1273Val
CA303550
NM_001202435.3:c.3818C>T