Canonical Allele Identifier: PA2825360264
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1193520
ClinVar RCV Id: RCV001555947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035233.1:p.Pro1622Leu
CA349037640
NM_001040143.2:c.4865C>T