Canonical Allele Identifier: PA2827756371
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 844965
ClinVar RCV Id: RCV001047939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Val229Leu
CA349074045
NM_001353949.2:c.685G>C