Canonical Allele Identifier: PA2741974585
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2924995
ClinVar RCV Id: RCV003780649
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Arg1586His
CA349036743
NM_021007.3:c.4757G>A