Canonical Allele Identifier: PA266849
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 93656
ClinVar RCV Id: RCV000079588 RCV001823112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Met1714Thr
CA266846
NM_001165963.4:c.5141T>C