Canonical Allele Identifier: PA2827761029
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1477591
ClinVar RCV Id: RCV001971669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Met1654Thr
CA349069821
NM_001353949.2:c.4961T>C