Canonical Allele Identifier: PA2827788941
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189968
ClinVar RCV Id: RCV000180922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Thr1271Arg
CA303438
NM_001353960.2:c.3812C>G