Canonical Allele Identifier: PA2827767633
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189845
ClinVar RCV Id: RCV000180799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Pro1657Arg
CA303095
NM_001353950.2:c.4970C>G