Canonical Allele Identifier: PA2827789574
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189922

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Ser1637Phe
CA303314
NM_001353960.2:c.4910C>T