Canonical Allele Identifier: PA2499287584
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1070304
ClinVar RCV Id: RCV001382401 RCV002319707
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Ala263Thr
CA349018089
NM_021007.3:c.787G>A