Canonical Allele Identifier: PA2826010580
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2203176
ClinVar RCV Id: RCV002664262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Met1555Arg
CA349072190
NM_001165963.4:c.4664T>G