Canonical Allele Identifier: PA2827767117
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1066555
ClinVar RCV Id: RCV001377575
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Pro1508Ser
CA349048587
NM_001353950.2:c.4522C>T