Canonical Allele Identifier: PA2828472867
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2009829
ClinVar RCV Id: RCV002842714
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Leu1624Pro
CA349037660
NM_001371246.1:c.4871T>C