Canonical Allele Identifier: PA2827777442
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Pro1507Thr
CA317497
NM_001353954.2:c.4519C>A