Canonical Allele Identifier: PA645402884
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 373136
ClinVar RCV Id: RCV000413989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Cys345Phe
CA16042370
NM_006920.6:c.1034G>T