Canonical Allele Identifier: PA2827783206
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 856106
ClinVar RCV Id: RCV001061500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Phe1387Ser
CA349049945
NM_001353957.2:c.4160T>C