Canonical Allele Identifier: PA2827785969
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2153965
ClinVar RCV Id: RCV003069036
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Leu1271Ser
CA1942866
NM_001353958.2:c.3812T>C