Canonical Allele Identifier: PA2825497306
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1215136
ClinVar RCV Id: RCV001583962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Phe1837Ser
CA352140834
NM_001099405.2:c.5510T>C