Canonical Allele Identifier: PA2828472524
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1804532
ClinVar RCV Id: RCV002469833 RCV002573599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Asn1475Lys
CA349034269
NM_001371246.1:c.4425C>A
CA349034271
NM_001371246.1:c.4425C>G