Canonical Allele Identifier: PA2827789172
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 836631
ClinVar RCV Id: RCV001037807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Lys1403Ile
CA349049621
NM_001353960.2:c.4208A>T