Canonical Allele Identifier: PA2827760632
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1067239
ClinVar RCV Id: RCV001378447

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Ile1534Lys
CA349072268
NM_001353949.2:c.4601T>A