Canonical Allele Identifier: PA2825944621
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 406448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Arg1121His
CA061975
NM_001160161.2:c.3362G>A