Canonical Allele Identifier: PA2828475009
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2435682
ClinVar RCV Id: RCV003136432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Asp927Tyr
CA349015491
NM_001371247.1:c.2779G>T