Canonical Allele Identifier: PA2825943916
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67698
ClinVar Variation Id: 67699
ClinVar RCV Id: RCV000058463

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Gly639Arg
CA015554
NM_001160161.2:c.1915G>A
CA015563
NM_001160161.2:c.1915G>C