Canonical Allele Identifier: PA2829675955
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 856106
ClinVar RCV Id: RCV001061500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Phe1404Ser
CA349049945
NM_006920.6:c.4211T>C