Canonical Allele Identifier: PA2828475308
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1407644
ClinVar RCV Id: RCV001909313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358176.1:p.Tyr1092Phe
CA349021652
NM_001371247.1:c.3275A>T