Canonical Allele Identifier: PA2827774016
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 167638
ClinVar RCV Id: RCV000153887
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Lys1259Asn
CA234845
NM_001353952.2:c.3777A>C
CA349054259
NM_001353952.2:c.3777A>T