Canonical Allele Identifier: PA2827773063
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1305332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Ser551Phe
CA349068255
NM_001353952.2:c.1652C>T