Canonical Allele Identifier: PA2827774460
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1466998
ClinVar RCV Id: RCV001990657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Pro1508Ala
CA349048588
NM_001353952.2:c.4522C>G