Canonical Allele Identifier: PA2825355433
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2945553
ClinVar RCV Id: RCV003803647
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Tyr1092His
CA349021646
NM_001040142.2:c.3274T>C