Canonical Allele Identifier: PA2826013731
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 408926
ClinVar RCV Id: RCV000460126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Met1636Thr
CA16610239
NM_001165964.3:c.4907T>C