Canonical Allele Identifier: PA2580229862
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2061575
ClinVar RCV Id: RCV002942835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Phe601Leu
CA349049943
NM_001353961.2:c.1803T>G
CA349049944
NM_001353961.2:c.1803T>A
CA349049949
NM_001353961.2:c.1801T>C