Canonical Allele Identifier: PA266848
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_008851.3:p.Met1703Thr
CA266846
NM_006920.6:c.5108T>C