Canonical Allele Identifier: PA2827774456
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Pro1508Thr
CA317497
NM_001353952.2:c.4522C>A