Canonical Allele Identifier: PA2825945349
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1189625
ClinVar RCV Id: RCV001550047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Gly1585Glu
CA352142972
NM_001160161.2:c.4754G>A