Canonical Allele Identifier: PA2827782108
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 375511
ClinVar RCV Id: RCV000417000
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Glu616Asp
CA16044314
NM_001353957.2:c.1848G>C
CA349067460
NM_001353957.2:c.1848G>T