Canonical Allele Identifier: PA2827779277
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Pro756Leu
CA303333
NM_001353955.2:c.2267C>T