Canonical Allele Identifier: PA2827788928
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 836073
ClinVar RCV Id: RCV001037109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Val1265Phe
CA349053549
NM_001353960.2:c.3793G>T