Canonical Allele Identifier: PA265026
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Asn70Lys
CA015856
NM_000335.5:c.210T>G
CA352158137
NM_000335.5:c.210T>A