Canonical Allele Identifier: PA2825356883
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 633560
ClinVar RCV Id: RCV000782070

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035232.1:p.Pro1622Arg
CA349037638
NM_001040142.2:c.4865C>G