Canonical Allele Identifier: PA2826012718
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 449377
ClinVar RCV Id: RCV000522963 RCV001315158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Asp978Glu
CA1943019
NM_001165964.3:c.2934T>G
CA349060373
NM_001165964.3:c.2934T>A