Canonical Allele Identifier: PA2826013533
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 429417
ClinVar RCV Id: RCV000493824
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Asp1516His
CA349072277
NM_001165964.3:c.4546G>C