Canonical Allele Identifier: PA658805784
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 521180
ClinVar RCV Id: RCV000622964
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Ala34Val
CA349009970
NM_021007.3:c.101C>T