Canonical Allele Identifier: PA2827774266
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 986202
ClinVar RCV Id: RCV001267495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Asn1406Ile
CA349049929
NM_001353952.2:c.4217A>T