Canonical Allele Identifier: PA2825491300
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1215136
ClinVar RCV Id: RCV001583962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Phe1855Ser
CA352140834
NM_001099404.2:c.5564T>C