Canonical Allele Identifier: PA2827774292
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2012859
ClinVar RCV Id: RCV002843428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Thr1419Ser
CA349049638
NM_001353952.2:c.4255A>T