Canonical Allele Identifier: PA2825942713
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1000020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Glu1843Val
CA352140568
NM_001160160.2:c.5528A>T