Canonical Allele Identifier: PA645406970
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 378927
ClinVar RCV Id: RCV000436956 RCV001042388 RCV001848748 RCV002267611 RCV001848747 RCV002281573 RCV003155938 RCV003441147 RCV002319492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Val261Met
CA16604008
NM_021007.3:c.781G>A