Canonical Allele Identifier: PA2827788980
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1064821
ClinVar RCV Id: RCV001374977 RCV001385510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Ala1297Asp
CA349052971
NM_001353960.2:c.3890C>A