Canonical Allele Identifier: PA2827789354
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 93653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Asn1499Lys
CA221595
NM_001353960.2:c.4497C>A
CA349072381
NM_001353960.2:c.4497C>G