Canonical Allele Identifier: PA2827780009
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2866808
ClinVar RCV Id: RCV003752705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Ala1271Gly
CA349053999
NM_001353955.2:c.3812C>G