Canonical Allele Identifier: PA2826012907
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1969094
ClinVar RCV Id: RCV002755344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Pro1149del
CA2580064350
NM_001165964.3:c.3445_3447del