Canonical Allele Identifier: PA2827922150
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Leu669Pro
CA352144988
NM_001354701.2:c.2006T>C