Canonical Allele Identifier: PA2827788332
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189949

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Ser843Tyr
CA303383
NM_001353960.2:c.2528C>A