Canonical Allele Identifier: PA2826011956
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206935
ClinVar RCV Id: RCV000189079
ClinVar Variation Id: 2846673
ClinVar RCV Id: RCV003754649
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Phe402Leu
CA317779
NM_001165964.3:c.1204T>C
CA349070981
NM_001165964.3:c.1206T>G
CA349070982
NM_001165964.3:c.1206T>A