Canonical Allele Identifier: PA2499287637
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1180106
ClinVar RCV Id: RCV001537239
ClinVar Variation Id: 1308640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Gln1479His
CA349034361
NM_021007.3:c.4437G>C
CA349034362
NM_021007.3:c.4437G>T