Canonical Allele Identifier: PA2827789401
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2651496
ClinVar RCV Id: RCV003429347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Asp1534His
CA349072056
NM_001353960.2:c.4600G>C