Canonical Allele Identifier: PA2827767209
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 546140
ClinVar RCV Id: RCV000657975 RCV002536319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Ile1540Phe
CA349072227
NM_001353950.2:c.4618A>T