Canonical Allele Identifier: PA2825944878
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1409689
ClinVar RCV Id: RCV003657448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Cys1287Arg
CA352147447
NM_001160161.2:c.3859T>C