Canonical Allele Identifier: PA2828472527
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2923538
ClinVar RCV Id: RCV003783096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Phe1476Leu
CA349034275
NM_001371246.1:c.4426T>C
CA349034303
NM_001371246.1:c.4428C>A
CA349034305
NM_001371246.1:c.4428C>G