Canonical Allele Identifier: PA2827781000
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1685088
ClinVar RCV Id: RCV002248180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Pro1832Leu
CA349065582
NM_001353955.2:c.5495C>T