Canonical Allele Identifier: PA2741980883
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 3053550
ClinVar RCV Id: RCV003985664
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Ala980Pro
CA349019399
NM_021007.3:c.2938G>C