Canonical Allele Identifier: PA265027
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Asn70Lys
CA015856
NM_001099404.2:c.210T>G
CA352158137
NM_001099404.2:c.210T>A