Canonical Allele Identifier: PA2827774020
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 593636
ClinVar RCV Id: RCV000728735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Tyr1263Cys
CA349054188
NM_001353952.2:c.3788A>G