Canonical Allele Identifier: PA221597
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 93653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Asn1517Lys
CA221595
NM_006920.6:c.4551C>A
CA349072381
NM_006920.6:c.4551C>G