Canonical Allele Identifier: PA2828471875
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 984816
ClinVar RCV Id: RCV001265270 RCV003313203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Glu1133Asp
CA349022082
NM_001371246.1:c.3399G>C
CA349022083
NM_001371246.1:c.3399G>T