Canonical Allele Identifier: PA2827756732
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206755
ClinVar RCV Id: RCV000188856 RCV000677680 RCV000986909
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Gly329Val
CA317185
NM_001353949.2:c.986G>T