Canonical Allele Identifier: PA2827789359
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 853086
ClinVar RCV Id: RCV001057828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Met1504Lys
CA349072346
NM_001353960.2:c.4511T>A