Canonical Allele Identifier: PA2825945443
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67955
ClinVar RCV Id: RCV000058740
ClinVar Variation Id: 2857136
ClinVar RCV Id: RCV003696758

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Gln1652His
CA018890
NM_001160161.2:c.4956G>C
CA352142300
NM_001160161.2:c.4956G>T