Canonical Allele Identifier: PA2827789143
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 986202
ClinVar RCV Id: RCV001267495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Asn1388Ile
CA349049929
NM_001353960.2:c.4163A>T