Canonical Allele Identifier: PA2827752941
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2092053
ClinVar RCV Id: RCV003008111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Tyr1279Cys
CA349054084
NM_001353948.2:c.3836A>G