Canonical Allele Identifier: PA2826013045
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2861060
ClinVar RCV Id: RCV003752614

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Ile1236Thr
CA349054333
NM_001165964.3:c.3707T>C