Canonical Allele Identifier: PA307219
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Arg367Cys
CA014305
NM_000335.5:c.1099C>T
CA645519439
NM_000335.5:c.1098_1099delinsTT