Canonical Allele Identifier: PA2827783007
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1505698
ClinVar RCV Id: RCV001999575
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Ser1270Thr
CA349053473
NM_001353957.2:c.3809G>C