Canonical Allele Identifier: PA2827773304
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Pro757Leu
CA303333
NM_001353952.2:c.2270C>T