Canonical Allele Identifier: PA2827777668
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68643
ClinVar RCV Id: RCV000059523 RCV000529623
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Thr1646Met
CA285192
NM_001353954.2:c.4937C>T