Canonical Allele Identifier: PA2573089150
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1305332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Ser551Phe
CA349068255
NM_006920.6:c.1652C>T