Canonical Allele Identifier: PA2826011581
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68575

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Asp194Asn
CA285033
NM_001165964.3:c.580G>A