Canonical Allele Identifier: PA2827780631
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 12882
ClinVar RCV Id: RCV000013742 RCV000059521 RCV000484119 RCV001040793 RCV001192959
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Arg1636His
CA256584
NM_001353955.2:c.4907G>A