Canonical Allele Identifier: PA2827785308
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189971
ClinVar RCV Id: RCV000180925

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Tyr799Asp
CA303448
NM_001353958.2:c.2395T>G