Canonical Allele Identifier: PA2827921737
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67648
ClinVar Variation Id: 67649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Asn406Lys
CA014532
NM_001354701.2:c.1218C>A
CA014540
NM_001354701.2:c.1218C>G