Canonical Allele Identifier: PA2827783640
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Met1637Ile
CA317565
NM_001353957.2:c.4911G>A
CA349069812
NM_001353957.2:c.4911G>T
CA349069815
NM_001353957.2:c.4911G>C