Canonical Allele Identifier: PA1139725153
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 994949
ClinVar RCV Id: RCV001288733
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Ala980Gly
CA349019403
NM_021007.3:c.2939C>G