Canonical Allele Identifier: PA285044
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Thr226Met
CA285042
NM_006920.6:c.677C>T