Canonical Allele Identifier: PA645404904
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 408926
ClinVar RCV Id: RCV000460126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Met1664Thr
CA16610239
NM_001165963.4:c.4991T>C