Canonical Allele Identifier: PA2826011636
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68579
ClinVar RCV Id: RCV000059455 RCV000636408 RCV000188842
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Ile227Ser
CA285045
NM_001165964.3:c.680T>G