Canonical Allele Identifier: PA2827788940
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2153965
ClinVar RCV Id: RCV003069036
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Leu1270Ser
CA1942866
NM_001353960.2:c.3809T>C