Canonical Allele Identifier: PA2828475959
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 3027168
ClinVar RCV Id: RCV003887561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Pro1441Arg
CA349033634
NM_001371247.1:c.4322C>G