Canonical Allele Identifier: PA2828470231
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2307995
ClinVar RCV Id: RCV002884267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Gln3His
CA349009640
NM_001371246.1:c.9G>C
CA349009642
NM_001371246.1:c.9G>T