Canonical Allele Identifier: PA916055803
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 644178
ClinVar RCV Id: RCV000798043
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066287.2:p.Pro360Ser
CA349020500
NM_021007.3:c.1078C>T