Canonical Allele Identifier: PA2826010377
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2015187
ClinVar RCV Id: RCV002839333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Phe1431Leu
CA349049627
NM_001165963.4:c.4293C>A
CA349049628
NM_001165963.4:c.4293C>G
CA349049633
NM_001165963.4:c.4291T>C