Canonical Allele Identifier: PA2828470720
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 644178
ClinVar RCV Id: RCV000798043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358175.1:p.Pro360Ser
CA349020500
NM_001371246.1:c.1078C>T