Canonical Allele Identifier: PA1139741155
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 853086
ClinVar RCV Id: RCV001057828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Met719Lys
CA349072346
NM_001353961.2:c.2156T>A