Canonical Allele Identifier: PA2826014004
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1205475
ClinVar RCV Id: RCV001572148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Met1779Ile
CA349067667
NM_001165964.3:c.5337G>T
CA349067669
NM_001165964.3:c.5337G>C
CA349067671
NM_001165964.3:c.5337G>A