Canonical Allele Identifier: PA2827752915
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 93647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Ala1273Pro
CA221583
NM_001353948.2:c.3817G>C